A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608332



Internal ID20981403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:897507..980251hg38UCSC Ensembl
chr7:937144..1019887hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3882745
hg1982744
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18160541
Samples
Known GenesADAP1, COX19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608332
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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