A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3968916



Internal ID19235007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:101241792..101244073hg38UCSC Ensembl
Outerchr13:101894143..101896424hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg382282
hg192282
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1113597
Supporting Variants
SamplesKWS2
Known GenesNALCN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3968916
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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