A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545844



Internal ID15986567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25276433..25300841hg38UCSC Ensembl
Innerchr1:25602924..25627332hg19UCSC Ensembl
Innerchr1:25475511..25499919hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3824409
hg1924409
hg1824409
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv711771
Samples
Known GenesRHD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545844
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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