A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17982779



Internal ID20549819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:61432601..61435000hg38UCSC Ensembl
chr10:63192359..63194758hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6453814
Supporting Variants
Samples
Known GenesTMEM26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17982779
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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