A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3656n106



Internal ID22797484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:121491416..121491486hg38UCSC Ensembl
chr7:121131470..121131540hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1128362, nsv1115002
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3656n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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