A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1625n106



Internal ID22795453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:65865997..65866386hg38UCSC Ensembl
chr18:63533233..63533622hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38390
hg19390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1112245, nsv1126384, nsv1130376, nsv1111534
SamplesKWS2, KWS1
Known GenesCDH7
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1625n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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