A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18141505



Internal ID20708545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151524973..151526263hg38UCSC Ensembl
chr6:151846108..151847398hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381291
hg191291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6606897
Supporting Variants
Samples
Known GenesCCDC170
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18141505
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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