A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3982323



Internal ID18865214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:39150811..39340215hg38UCSC Ensembl
Outerchr9:65524800..65584900hg19UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38189405
hg1960101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1145237
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3982323
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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