A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1117679



Internal ID18925243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:158811304..158811361hg38UCSC Ensembl
Outerchr6:159232336..159232393hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3957786
SamplesKWS1
Known GenesEZR
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1117679
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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