A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058579



Internal ID18801110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:7768804..7820978hg38UCSC Ensembl
Innerchr19:7833690..7885864hg19UCSC Ensembl
Innerchr19:7739690..7791864hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3852175
hg1952175
hg1852175
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564673
Samples
Known GenesCLEC4GP1, CLEC4M
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058579
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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