A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574337



Internal ID16361746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:8311399..8354295hg38UCSC Ensembl
Innerchr17:8214717..8257613hg19UCSC Ensembl
Innerchr17:8155442..8198338hg18UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3842897
hg1942897
hg1842897
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149691
Samples1780862084_A
Known GenesARHGEF15, ODF4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574337
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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