A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998934



Internal ID18811784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:15053249..15172736hg38UCSC Ensembl
Innerchr3:15094756..15214243hg19UCSC Ensembl
Innerchr3:15069760..15189247hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38119488
hg19119488
hg18119488
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4687n100
Supporting Variantsnssv3593091, nssv3739636, nssv3593090
Samples
Known GenesCOL6A4P1, MRPS25, ZFYVE20
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998934
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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