A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1143235



Internal ID19264924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:126597200..126597263hg38UCSC Ensembl
Outerchr9:129359479..129359542hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3988438, nssv3984186
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1143235
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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