A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3982305



Internal ID19205771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:60874228..60897828hg38UCSC Ensembl
Outerchr9:41460500..41484100hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3823601
hg1923601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1145219
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3982305
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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