A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1077689



Internal ID15930875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:192140..193461hg38UCSC Ensembl
Innerchr7:192140..193461hg19UCSC Ensembl
Innerchr7:287223..288544hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg381322
hg191322
hg181322
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605624
Supporting Variants
Samples
Known GenesFAM20C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1077689
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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