A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3626n106



Internal ID20162983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:100949668..100962871hg38UCSC Ensembl
chr7:100547300..100554700hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3813204
hg197401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1115758, nsv1132653
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3626n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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