A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150988



Internal ID18856095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:158802943..158803602hg38UCSC Ensembl
Outerchr6:159223975..159224634hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38660
hg19660
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4001921
SamplesKWB1
Known GenesEZR
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150988
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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