A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18152483



Internal ID20719523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:14332076..14332416hg38UCSC Ensembl
chr7:14371701..14372041hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6605612
Supporting Variants
Samples
Known GenesDGKB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18152483
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00076


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