A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407282



Internal ID21064835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:55864448..55865074hg38UCSC Ensembl
chr6:55729246..55729872hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38627
hg19627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18145854
Samples
Known GenesBMP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407282
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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