A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1109646



Internal ID19273771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:148785241..148785340hg38UCSC Ensembl
Outerchr4:149706393..149706492hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3957182
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1109646
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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