A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1077696



Internal ID15930882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:206660..207348hg38UCSC Ensembl
Innerchr7:206660..207348hg19UCSC Ensembl
Innerchr7:301743..302431hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38689
hg19689
hg18689
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605631
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)nssv1077696
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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