A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011352



Internal ID18753886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:15053249..15177840hg38UCSC Ensembl
Innerchr3:15094756..15219347hg19UCSC Ensembl
Innerchr3:15069760..15194351hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38124592
hg19124592
hg18124592
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4687n100
Supporting Variantsnssv3593092
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)nsv1011352
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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