A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1129034



Internal ID19255800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:67855254..67857554hg38UCSC Ensembl
Outerchr9:67922700..67925000hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg382301
hg192301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3961707
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1129034
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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