A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000899



Internal ID19090116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:57310682..57467007hg38UCSC Ensembl
Innerchr2:57537817..57694142hg19UCSC Ensembl
Innerchr2:57391321..57547646hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38156326
hg19156326
hg18156326
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3730849
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)nsv1000899
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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