A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1091196



Internal ID15597696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:95410668..95414211hg38UCSC Ensembl
Innerchr7:95039980..95043523hg19UCSC Ensembl
Innerchr7:94877916..94881459hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg383544
hg193544
hg183544
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607863
Supporting Variants
Samples
Known GenesPON2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1091196
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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