A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6632n223



Internal ID22809600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:29628701..29659200hg38UCSC Ensembl
chr7:29668317..29698816hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3830500
hg1930500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6614663, nsv6610787
Samples
Known GenesLOC646762
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6632n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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