A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979416



Internal ID20546456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:36023201..36201500hg38UCSC Ensembl
chr10:36312129..36490428hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38178300
hg19178300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443862
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979416
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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