A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv719678



Internal ID15666948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:101810587..101838538hg38UCSC Ensembl
Innerchr1:102276143..102304094hg19UCSC Ensembl
Innerchr1:102048731..102076682hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3827952
hg1927952
hg1827952
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546899
Supporting Variants
Samples
Known GenesOLFM3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv719678
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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