A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6003679



Internal ID8981082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:71493479..71494786hg38UCSC Ensembl
chr7:70958464..70959771hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg381308
hg191308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2662410
Supporting Variants
SamplesNA20819
Known GenesWBSCR17
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6003679
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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