A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155930



Internal ID15875451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:156063427..156091774hg38UCSC Ensembl
Innerchr7:155856121..155884468hg19UCSC Ensembl
Innerchr7:155548882..155577229hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3828348
hg1928348
hg1828348
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv609167
Supporting Variants
SamplesHGDP00684
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155930
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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