A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17978149



Internal ID20545189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112891432..112897994hg38UCSC Ensembl
chr10:114651191..114657753hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg386563
hg196563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454643
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17978149
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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