A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013878



Internal ID19103097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:207475654..207495060hg38UCSC Ensembl
Innerchr2:208340378..208359784hg19UCSC Ensembl
Innerchr2:208048623..208068029hg18UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg3819407
hg1919407
hg1819407
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4157n100
Supporting Variantsnssv3585587
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)nsv1013878
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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