A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17981393



Internal ID20548433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:30304391..30309807hg38UCSC Ensembl
chr10:30593320..30598736hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg385417
hg195417
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439956
Supporting Variants
Samples
Known GenesMTPAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17981393
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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