A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17980421



Internal ID20547461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45648189..45656373hg38UCSC Ensembl
chr10:46143637..46151821hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg388185
hg198185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454788
Supporting Variants
Samples
Known GenesZFAND4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17980421
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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