A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658442



Internal ID9924547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156531938..156542821hg38UCSC Ensembl
chr7:156324632..156335515hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3810884
hg1910884
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6459932, essv5415263, essv5957427, essv6350142, essv5884729
SamplesNA19397, NA19390, NA19439, NA19430, NA19463
Known GenesLINC00244, LINC01006
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658442
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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