A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1136071



Internal ID18910719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:25295209..25301609hg38UCSC Ensembl
Outerchr1:25621700..25628100hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg386401
hg196401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3989678
SamplesKWS2
Known GenesRHD
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1136071
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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