A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001575



Internal ID19090792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:4158085..4176417hg38UCSC Ensembl
Innerchr2:4205675..4224007hg19UCSC Ensembl
Innerchr2:4183550..4201882hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3818333
hg1918333
hg1818333
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3704n100
Supporting Variantsnssv3726669, nssv3571368, nssv3571365, nssv3571363, nssv3571364, nssv3571361, nssv3571362, nssv3571366, nssv3571369, nssv3571358, nssv3571367, nssv3571360, nssv3571359
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)nsv1001575
Frequency
Sample Size11257
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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