A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17984011



Internal ID20551051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74671560..74672473hg38UCSC Ensembl
chr10:76431318..76432231hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38914
hg19914
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440766
Supporting Variants
Samples
Known GenesADK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17984011
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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