A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18082955



Internal ID20649995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206297961..206299117hg38UCSC Ensembl
chr2:207162685..207163841hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg381157
hg191157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6351028
Supporting Variants
Samples
Known GenesZDBF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18082955
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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