A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011645



Internal ID19100862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65203760..65230894hg38UCSC Ensembl
Innerchr3:65189435..65216569hg19UCSC Ensembl
Innerchr3:65164475..65191609hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3827135
hg1927135
hg1827135
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4762n100
Supporting Variantsnssv3593893, nssv3593892, nssv3593894
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)nsv1011645
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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