A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549399



Internal ID15990122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:236129368..236151770hg38UCSC Ensembl
Innerchr1:236292668..236315070hg19UCSC Ensembl
Innerchr1:234359291..234381693hg18UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg3822403
hg1922403
hg1822403
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv738184
Samples
Known GenesGPR137B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549399
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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