A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998571



Internal ID19158107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21212781..21297884hg38UCSC Ensembl
Innerchr3:21254273..21339376hg19UCSC Ensembl
Innerchr3:21229277..21314380hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3885104
hg1985104
hg1885104
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4690n100
Supporting Variantsnssv3739645, nssv3593121
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)nsv998571
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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