A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002112



Internal ID19091329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:191677980..191753213hg38UCSC Ensembl
Innerchr3:191395769..191471002hg19UCSC Ensembl
Innerchr3:192878463..192953696hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3875234
hg1975234
hg1875234
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3738460
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)nsv1002112
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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