A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174060



Internal ID15873614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:236121000..236194091hg38UCSC Ensembl
Innerchr1:236284300..236357391hg19UCSC Ensembl
Innerchr1:234350923..234424014hg18UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg3873092
hg1973092
hg1873092
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549397
Supporting Variants
SamplesHGDP00264
Known GenesGPR137B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174060
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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