A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545838



Internal ID15986561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25271785..25333196hg38UCSC Ensembl
Innerchr1:25598276..25659687hg19UCSC Ensembl
Innerchr1:25470863..25532274hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3861412
hg1961412
hg1861412
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv201n54
Supporting Variantsnssv711737, nssv711731, nssv711735, nssv711740, nssv711736, nssv711738, nssv711739, nssv711733, nssv711734, nssv711732, nssv711730
Samples
Known GenesRHD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545838
Frequency
Sample Size17421
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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