A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979259



Internal ID20546299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24647893..24651115hg38UCSC Ensembl
chr10:24936822..24940044hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg383223
hg193223
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436523
Supporting Variants
Samples
Known GenesARHGAP21
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979259
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


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