A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612836



Internal ID20985907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:14063721..14145602hg38UCSC Ensembl
chr7:14103346..14185227hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3881882
hg1981882
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150703
Samples
Known GenesDGKB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612836
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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