A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319668



Internal ID20852763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:213078121..213080584hg38UCSC Ensembl
chr1:213251463..213253926hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg382464
hg192464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057730
Samples
Known GenesRPS6KC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319668
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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