A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2696n106



Internal ID20162053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:11800..68808hg38UCSC Ensembl
chr4:11800..68700hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3857009
hg1956901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1115660, nsv1132582
SamplesKWS1, KWS2
Known GenesZNF595, ZNF718
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2696n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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