A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18085517



Internal ID20652557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:219449776..219455202hg38UCSC Ensembl
chr2:220314498..220319924hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg385427
hg195427
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6350775
Supporting Variants
Samples
Known GenesSPEG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18085517
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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