A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412571



Internal ID21070124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:93200401..93201400hg38UCSC Ensembl
chr6:93910119..93911118hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18146781
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412571
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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