A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068135



Internal ID20635175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:51760629..51765526hg38UCSC Ensembl
chr20:50377168..50382065hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg384898
hg194898
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6544482
Supporting Variants
Samples
Known GenesATP9A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068135
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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