A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3999920



Internal ID19187035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:133549032..133549302hg38UCSC Ensembl
Outerchr9:136414154..136414424hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38271
hg19271
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1152742
Supporting Variants
SamplesKWB1
Known GenesADAMTSL2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3999920
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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