A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062173



Internal ID18804704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:1103206..1360460hg38UCSC Ensembl
Innerchr17:1006446..1263754hg19UCSC Ensembl
Innerchr17:953196..1210504hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38257255
hg19257309
hg18257309
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3081n100
Supporting Variantsnssv3560067
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)nsv1062173
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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