A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979168



Internal ID20546208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:3121305..3126563hg38UCSC Ensembl
chr10:3163497..3168755hg19UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg385259
hg195259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442625
Supporting Variants
Samples
Known GenesPFKP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979168
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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