A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411252



Internal ID21068805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:64252301..64271500hg38UCSC Ensembl
chr6:64962194..64981393hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3819200
hg1919200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143539
Samples
Known GenesEYS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411252
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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