A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1658n106



Internal ID20161015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:79521600..79522400hg38UCSC Ensembl
chr18:77281600..77282400hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1121957, nsv1143889
SamplesKWS1, KWS2
Known GenesNFATC1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1658n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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