A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18073315



Internal ID20640355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44647599..44648064hg38UCSC Ensembl
chr21:46067516..46067981hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38466
hg19466
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6543297
Supporting Variants
Samples
Known GenesKRTAP10-11, TSPEAR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18073315
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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