A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150789



Internal ID15875764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:159382207..159426465hg38UCSC Ensembl
Innerchr2:160238718..160282976hg19UCSC Ensembl
Innerchr2:159946964..159991222hg18UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg3844259
hg1944259
hg1844259
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv583496
Supporting Variants
SamplesHGDP00734
Known GenesBAZ2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150789
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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