A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002384



Internal ID19091601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:192501762..192664586hg38UCSC Ensembl
Innerchr2:193366488..193529312hg19UCSC Ensembl
Innerchr2:193074733..193237557hg18UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38162825
hg19162825
hg18162825
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4139n100
Supporting Variantsnssv3583901
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)nsv1002384
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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