A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062505



Internal ID19151724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:68082268..68189163hg38UCSC Ensembl
Innerchr17:66078392..66185304hg19UCSC Ensembl
Innerchr17:63590029..63696899hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38106896
hg19106913
hg18106871
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3277n100
Supporting Variantsnssv3725145
Samples
Known GenesLINC00674
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062505
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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