A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12745689



Internal ID6385065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:39152087..39209424hg38UCSC Ensembl
chr7:39191686..39249023hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3857338
hg1957338
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3612898
Supporting Variants
SamplesNA20321
Known GenesPOU6F2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12745689
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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