A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155924



Internal ID15878228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:154880936..154901904hg38UCSC Ensembl
Innerchr7:154672646..154693614hg19UCSC Ensembl
Innerchr7:154303579..154324547hg18UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3820969
hg1920969
hg1820969
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv609113
Supporting Variants
SamplesHGDP01163
Known GenesDPP6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155924
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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