A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18080412



Internal ID20647453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:172237841..172243720hg38UCSC Ensembl
chr2:173102569..173108448hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg385880
hg195880
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6345929
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18080412
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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