A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv784n106



Internal ID22794612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25958267..25959067hg38UCSC Ensembl
chr12:26111200..26112000hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1112619, nsv1126314
SamplesKWS2, KWS1
Known GenesRASSF8, RASSF8-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv784n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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