A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217043



Internal ID20784083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167155513..167512188hg38UCSC Ensembl
chr6:167569001..167924380hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38356676
hg19355380
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6604858
Supporting Variants
Samples
Known GenesGPR31, TCP10, TCP10L2, TTLL2, UNC93A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217043
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00018


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