A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3987501



Internal ID18869807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:39092424..39097600hg38UCSC Ensembl
Outerchr9:65638200..65643400hg19UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg385177
hg195201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1132711
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3987501
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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