A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412963



Internal ID21070516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25169882..25177833hg38UCSC Ensembl
chr6:25170110..25178061hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg387952
hg197952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140682
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412963
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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