A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3719n106



Internal ID22797547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156264806..156267506hg38UCSC Ensembl
chr7:156057500..156060200hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg382701
hg192701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1139913, nsv1119240
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3719n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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