A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574127



Internal ID16361536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:949043..949686hg38UCSC Ensembl
Innerchr17:852283..852926hg19UCSC Ensembl
Innerchr17:799033..799676hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38644
hg19644
hg18644
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5398n54
Supporting Variantsnssv866149, nssv866148, nssv866142, nssv866139, nssv866145, nssv866137, nssv866143, nssv866141, nssv866140, nssv866146, nssv866147, nssv866151, nssv866138, nssv866150, nssv866144
Samples
Known GenesNXN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574127
Frequency
Sample Size17421
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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