A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663734



Internal ID9929839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:5896931..5911542hg38UCSC Ensembl
chr7:5936562..5951173hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3814612
hg1914612
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6444416, essv6304844, essv6268240, essv5870574, essv6164443, essv5663505, essv6152031, essv5503804, essv5583913, essv6079240, essv5570139, essv6238753, essv6518820, essv5814160, essv5511357, essv6324099, essv5939147, essv5888111, essv5868626, essv5681225, essv6044413, essv5657826, essv5949170, essv5939137, essv5533791, essv5506414, essv5715362, essv5922670, essv5873496, essv5690612, essv6317300, essv5446109, essv6377630, essv6030776, essv6034016, essv6388846, essv6383437, essv5456834, essv6464861, essv6171807
SamplesHG00403, HG00542, HG00442, HG00699, HG00566, HG00654, HG00702, HG00448, HG00610, HG00683, HG00534, HG00705, HG00427, HG00530, HG00560, HG00596, HG00557, HG00653, HG00657, HG00475, HG00500, HG00619, HG00692, HG00651, HG00684, HG00613, HG00525, HG00704, HG00611, HG00625, HG00473, HG00607, HG00620, HG00707, HG00672, HG00614, HG00513, HG00578, HG00421, HG00698
Known GenesCCZ1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663734
Frequency
Sample Size1151
Observed Gain0
Observed Loss40
Observed Complex0
Frequencyn/a


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