A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545687



Internal ID15986410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16919140..16935719hg38UCSC Ensembl
Innerchr1:17245635..17262214hg19UCSC Ensembl
Innerchr1:17118222..17134801hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3816580
hg1916580
hg1816580
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv171n54
Supporting Variantsnssv710918, nssv710917, nssv710916
Samples
Known GenesCROCC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545687
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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