A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18091140



Internal ID20658180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:85609888..85610293hg38UCSC Ensembl
chr2:85837011..85837416hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38406
hg19406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6354120
Supporting Variants
Samples
Known GenesC2orf68, USP39
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18091140
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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