A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3567791



Internal ID18519386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:73835799..74684903hg38UCSC Ensembl
Innerchr17:71831938..72681042hg19UCSC Ensembl
Innerchr17:69343533..70192637hg18UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38849105
hg19849105
hg18849105
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059520
Supporting Variants
Samples
Known GenesBTBD17, C17orf77, CD300A, CD300C, CD300E, CD300LB, CD300LD, DNAI2, GPR142, GPRC5C, KIF19, MGC16275, RAB37, RPL38, TTYH2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3567791
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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