A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5672496



Internal ID8772324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:65094951..65784399hg38UCSC Ensembl
chr7:64555329..65249386hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38689449
hg19694058
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2670004
Supporting Variants
SamplesHG00174
Known GenesCCT6P1, INTS4L2, LOC441242, SNORA22, ZNF92
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5672496
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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