A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3965242



Internal ID18874424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:96695580..96695668hg38UCSC Ensembl
Outerchr13:97347834..97347922hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1130090
Supporting Variants
SamplesKWS1
Known GenesHS6ST3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3965242
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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