A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413812



Internal ID21071365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:55830034..55830561hg38UCSC Ensembl
chr6:55694832..55695359hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38528
hg19528
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18145847
Samples
Known GenesBMP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413812
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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