A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1129037



Internal ID18903981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:63781666..63841366hg38UCSC Ensembl
Outerchr9:68377400..68437100hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3859701
hg1959701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4037n106
Supporting Variantsnssv3961710
SamplesKWS1
Known GenesLOC642236
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1129037
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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