A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607680



Internal ID16395089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:80468260..80512901hg38UCSC Ensembl
Innerchr7:80097576..80142217hg19UCSC Ensembl
Innerchr7:79935512..79980153hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3844642
hg1944642
hg1844642
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1088535
Samples
Known GenesGNAT3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607680
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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