A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411551



Internal ID21069104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:55863744..55864115hg38UCSC Ensembl
chr6:55728542..55728913hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38372
hg19372
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18145853
Samples
Known GenesBMP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411551
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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