A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv712364



Internal ID16006320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:37171821..37218318hg38UCSC Ensembl
Innerchr1:37637422..37683919hg19UCSC Ensembl
Innerchr1:37410009..37456506hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3846498
hg1946498
hg1846498
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546017
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv712364
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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