A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615745



Internal ID20988816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20667651..20669743hg38UCSC Ensembl
chr7:20707274..20709366hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg382093
hg192093
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18156909
Samples
Known GenesABCB5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615745
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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