A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2641n106



Internal ID22796469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177663512..177667625hg38UCSC Ensembl
chr3:177381300..177385413hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg384114
hg194114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1122420, nsv1132783
SamplesKWS1
Known GenesLINC00578
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2641n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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