A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3299n106



Internal ID20162656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35496523..35497423hg38UCSC Ensembl
chr6:35464300..35465200hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38901
hg19901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1122127, nsv1119080
SamplesKWS1, KWS2
Known GenesTEAD3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3299n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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