A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173834



Internal ID15855314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:40881556..40918166hg38UCSC Ensembl
Innerchr1:41347228..41383838hg19UCSC Ensembl
Innerchr1:41119815..41156425hg18UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3836611
hg1936611
hg1836611
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546098
Supporting Variants
Samples1780862551_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173834
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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