A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv226n106



Internal ID20159583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:179638146..179638965hg38UCSC Ensembl
chr1:179607281..179608100hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg38820
hg19820
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1120372, nsv1113196, nsv1132197
SamplesKWS1, KWS2
Known GenesTDRD5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv226n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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