A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3958840



Internal ID18865737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:99979176..99979238hg38UCSC Ensembl
Outerchr9:102741458..102741520hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1117898
Supporting Variants
SamplesKWS1
Known GenesERP44
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3958840
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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