A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3239n106



Internal ID19021348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:179277299..179278199hg38UCSC Ensembl
chr5:178704300..178705200hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38901
hg19901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1126735, nsv1133620
SamplesKWS1, KWS2
Known GenesADAMTS2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3239n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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