A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17980249



Internal ID20547289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:34539805..34600810hg38UCSC Ensembl
chr10:34828733..34889738hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3861006
hg1961006
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454468
Supporting Variants
Samples
Known GenesPARD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17980249
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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