A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576024



Internal ID16016747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:74450469..74673021hg38UCSC Ensembl
Innerchr17:72446608..72669160hg19UCSC Ensembl
Innerchr17:69958203..70180755hg18UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38222553
hg19222553
hg18222553
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5774n54
Supporting Variantsnssv876103
Samples
Known GenesC17orf77, CD300A, CD300C, CD300E, CD300LB, CD300LD, RAB37
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576024
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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