A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125055



Internal ID19261388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:41186371..41204971hg38UCSC Ensembl
Outerchr9:69259600..69278200hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3818601
hg1918601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3977861
SamplesKWS2
Known GenesCBWD5, CBWD6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125055
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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