A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574096



Internal ID16361505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:823892..875010hg38UCSC Ensembl
Innerchr17:727132..778250hg19UCSC Ensembl
Innerchr17:673882..725000hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3851119
hg1951119
hg1851119
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150562
SamplesNINDS_203
Known GenesNXN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574096
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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