A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067245



Internal ID19156464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:67134041..67184981hg38UCSC Ensembl
Innerchr17:65130157..65181097hg19UCSC Ensembl
Innerchr17:62560619..62611559hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3850941
hg1950941
hg1850941
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3567744
Samples
Known GenesHELZ
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067245
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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