A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18161961



Internal ID20729001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:88506708..88626927hg38UCSC Ensembl
chr7:88136023..88256241hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg38120220
hg19120219
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6603508
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18161961
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00033


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