A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602047



Internal ID20975118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20582638..20589594hg38UCSC Ensembl
chr7:20622261..20629217hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg386957
hg196957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18156901
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602047
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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