A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010400



Internal ID18752931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46790459..46818330hg38UCSC Ensembl
Innerchr3:46831949..46859820hg19UCSC Ensembl
Innerchr3:46806953..46834824hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3827872
hg1927872
hg1827872
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4738n100
Supporting Variantsnssv3595243
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)nsv1010400
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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