A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3578888



Internal ID18877169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:17039813..17061270hg38UCSC Ensembl
Innerchr2:17221080..17242537hg19UCSC Ensembl
Innerchr2:17084561..17106018hg18UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg3821458
hg1921458
hg1821458
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv997651
Supporting Variants
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)nssv3578888
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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