A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3419n106



Internal ID22797247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157278768..157282268hg38UCSC Ensembl
chr6:157699800..157703300hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg383501
hg193501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1110862, nsv1131597, nsv1121359, nsv1130250, nsv1111711
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3419n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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