A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173062



Internal ID15880324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:94656962..94677287hg38UCSC Ensembl
Innerchr1:95122518..95142843hg19UCSC Ensembl
Innerchr1:94895106..94915431hg18UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3820326
hg1920326
hg1820326
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546852
Supporting Variants
SamplesNINDS_196
Known GenesLINC01057
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173062
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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