A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18141654



Internal ID20708694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34407784..34409124hg38UCSC Ensembl
chr6:34375561..34376901hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg381341
hg191341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6398711
Supporting Variants
Samples
Known GenesRPS10-NUDT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18141654
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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