A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1119564



Internal ID19254446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:35952837..35952914hg38UCSC Ensembl
Outerchr9:35952834..35952911hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960764
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1119564
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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