A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002021



Internal ID19091238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:72066561..72268388hg38UCSC Ensembl
Innerchr3:72115712..72317539hg19UCSC Ensembl
Innerchr3:72198402..72400229hg18UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38201828
hg19201828
hg18201828
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3594158
Samples
Known GenesLINC00870, LINC00877
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1002021
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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