A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400665



Internal ID21058218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75095467..75096895hg38UCSC Ensembl
chr6:75805183..75806611hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg381429
hg191429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18145181
Samples
Known GenesCOL12A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400665
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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