A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412935



Internal ID21070488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63814641..63816816hg38UCSC Ensembl
chr6:64524534..64526709hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg382176
hg192176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18142992
Samples
Known GenesEYS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412935
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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