A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950324



Internal ID16952511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:25264110..25336209hg38UCSC Ensembl
Outerchr1:25590601..25662700hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3872100
hg1972100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997099
SamplesBILGI_BIOE
Known GenesRHD
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950324
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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