A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1642n106



Internal ID22795470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76492244..76495544hg38UCSC Ensembl
chr18:74204200..74207500hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg383301
hg193301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1126488, nsv1136256
SamplesKWS2, KWS1
Known GenesFLJ44313, ZNF516
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1642n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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