A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv958n106



Internal ID22794786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:39360045..39361376hg38UCSC Ensembl
chr13:39934182..39935513hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg381332
hg191332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1114617, nsv1120990, nsv1135460, nsv1120676
SamplesKWS2, KWS1
Known GenesLHFP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv958n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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