A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605991



Internal ID20979062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:9332976..9341883hg38UCSC Ensembl
chr7:9372606..9381513hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg388908
hg198908
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161769
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605991
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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