A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18080456



Internal ID20647497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:173173749..173175404hg38UCSC Ensembl
chr2:174038477..174040132hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg381656
hg191656
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6343211
Supporting Variants
Samples
Known GenesZAK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18080456
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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