A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150744



Internal ID15532629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:226136270..226157320hg38UCSC Ensembl
Innerchr2:227000986..227022036hg19UCSC Ensembl
Innerchr2:226709230..226730280hg18UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg3821051
hg1921051
hg1821051
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584559
Supporting Variants
SamplesHGDP01343
Known GenesLOC646736
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150744
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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