A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv28n106



Internal ID20159385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6235640..6236340hg38UCSC Ensembl
chr1:6295700..6296400hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1130943, nsv1118096
SamplesKWS1, KWS2
Known GenesICMT, LINC00337
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv28n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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