A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18144434



Internal ID20711474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:70285270..70286087hg38UCSC Ensembl
chr6:70994973..70995790hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38818
hg19818
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6414793
Supporting Variants
Samples
Known GenesCOL9A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18144434
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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