A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065010



Internal ID18807541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:1095450..1352208hg38UCSC Ensembl
Innerchr17:998690..1255502hg19UCSC Ensembl
Innerchr17:945440..1202252hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38256759
hg19256813
hg18256813
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3081n100
Supporting Variantsnssv3560066
Samples
Known GenesABR, BHLHA9, TUSC5, YWHAE
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065010
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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