A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1119089



Internal ID18919770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:157703868..157706768hg38UCSC Ensembl
Outerchr6:158124900..158127800hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg382901
hg192901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3981891
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1119089
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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