A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3999220



Internal ID19191111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:39360047..39361401hg38UCSC Ensembl
Outerchr13:39934184..39935538hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg381355
hg191355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1152038
Supporting Variants
SamplesKWB1
Known GenesLHFP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3999220
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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