A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612916



Internal ID20985987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:84353658..84483136hg38UCSC Ensembl
chr7:83982974..84112452hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38129479
hg19129479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161723
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612916
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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