A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1860n106



Internal ID20161217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:8678470..8679170hg38UCSC Ensembl
chr2:8818600..8819300hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1136293, nsv1144890
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1860n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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