A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1764n106



Internal ID22795592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30130690..30130813hg38UCSC Ensembl
chr19:30621597..30621720hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1123246, nsv1144833
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1764n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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