A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545835



Internal ID16333244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25271785..25314890hg38UCSC Ensembl
Innerchr1:25598276..25641381hg19UCSC Ensembl
Innerchr1:25470863..25513968hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3843106
hg1943106
hg1843106
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv203n54
Supporting Variantsnssv711703, nssv711700, nssv711702, nssv711704, nssv711701
Samples
Known GenesRHD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545835
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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