A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062574



Internal ID19151793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:18452066..18626748hg38UCSC Ensembl
Innerchr17:18355380..18530061hg19UCSC Ensembl
Innerchr17:18296105..18470786hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38174683
hg19174682
hg18174682
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3115n100
Supporting Variantsnssv3560526, nssv3560527
Samples
Known GenesCCDC144B, FAM106A, LGALS9C, USP32P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062574
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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