A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1119616



Internal ID19252591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:136808148..136808648hg38UCSC Ensembl
Outerchr9:139702600..139703100hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3982053
SamplesKWS1
Known GenesCCDC183-AS1, RABL6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1119616
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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