A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18088651



Internal ID20655691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:44448901..44449500hg38UCSC Ensembl
chr2:44676040..44676639hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6351916
Supporting Variants
Samples
Known GenesCAMKMT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18088651
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00032


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