A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3725145



Internal ID19023426
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 StatusS
Merged Variantsnsv1062505
Supporting Variants
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)nssv3725145
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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