A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574101



Internal ID16361510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:915281..940637hg38UCSC Ensembl
Innerchr17:818521..843877hg19UCSC Ensembl
Innerchr17:765271..790627hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3825357
hg1925357
hg1825357
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv865847
Samples
Known GenesNXN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574101
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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