A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3982046



Internal ID19216558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:133551778..133588478hg38UCSC Ensembl
Outerchr9:136416900..136453600hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3836701
hg1936701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1119612
Supporting Variants
SamplesKWS1
Known GenesADAMTSL2, FAM163B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3982046
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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