A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604858



Internal ID20977929
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 StatusM
Merged Variants
Supporting Variantsnssv18217043
Samples
Known GenesGPR31, TCP10, TCP10L2, TTLL2, UNC93A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604858
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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