A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1191n106



Internal ID22795019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:37812552..37812663hg38UCSC Ensembl
chr15:38104753..38104864hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1120698, nsv1121149
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1191n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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