A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010960



Internal ID19100177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12269..36319hg38UCSC Ensembl
Innerchr4:12269..36319hg19UCSC Ensembl
Innerchr4:2269..26319hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3824051
hg1924051
hg1824051
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5050n100
Supporting Variantsnssv3617063, nssv3617059, nssv3617056, nssv3617055, nssv3617060, nssv3617058, nssv3617062, nssv3737886, nssv3617061, nssv3617057
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)nsv1010960
Frequency
Sample Size11257
Observed Gain2
Observed Loss8
Observed Complex0
Frequencyn/a


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