A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3679n106



Internal ID20163036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141414063..141414384hg38UCSC Ensembl
chr7:141113863..141114184hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1130568, nsv1135250
SamplesKWS1, KWS2
Known GenesTMEM178B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3679n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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