A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960378



Internal ID19217274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:72578281..72578331hg38UCSC Ensembl
Outerchr9:75193197..75193247hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1128497
Supporting Variants
SamplesKWS1
Known GenesTMC1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960378
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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