A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058388



Internal ID19147607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:52430155..52588685hg38UCSC Ensembl
Innerchr17:50507515..50666045hg19UCSC Ensembl
Innerchr17:47862514..48021044hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38158531
hg19158531
hg18158531
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3568610
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)nsv1058388
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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