A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009161



Internal ID19098379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:52070754..52253044hg38UCSC Ensembl
Innerchr2:52297892..52480182hg19UCSC Ensembl
Innerchr2:52151396..52333686hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg38182291
hg19182291
hg18182291
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3726031
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009161
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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