A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614520



Internal ID20987591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108324925..108330335hg38UCSC Ensembl
chr6:108646129..108651539hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg385411
hg195411
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136988
Samples
Known GenesLACE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614520
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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