A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010501



Internal ID19099718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:4155585..4172341hg38UCSC Ensembl
Innerchr2:4203175..4219931hg19UCSC Ensembl
Innerchr2:4181050..4197806hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3816757
hg1916757
hg1816757
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3704n100
Supporting Variantsnssv3571306
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)nsv1010501
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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