A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959242



Internal ID19210787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:62799077..62799144hg38UCSC Ensembl
Outerchr9:66454901..66454968hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110016
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959242
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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