A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18084057



Internal ID20651097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:215705219..215739749hg38UCSC Ensembl
chr2:216569942..216604472hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3834531
hg1934531
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6354054
Supporting Variants
Samples
Known GenesLINC00607
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18084057
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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