A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150764



Internal ID15508335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:233333701..233379402hg38UCSC Ensembl
Innerchr2:234242347..234288048hg19UCSC Ensembl
Innerchr2:233907086..233952787hg18UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3845702
hg1945702
hg1845702
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584701
Supporting Variants
Samples1780862415_A
Known GenesDGKD, SAG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150764
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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