A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010204



Internal ID18752735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4028129..4112924hg38UCSC Ensembl
Innerchr3:4069813..4154608hg19UCSC Ensembl
Innerchr3:4044813..4129608hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3884796
hg1984796
hg1884796
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4642n100
Supporting Variantsnssv3590408
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)nsv1010204
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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