A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615509



Internal ID20988580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:133517012..133518183hg38UCSC Ensembl
chr6:133838150..133839321hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg381172
hg191172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139377
Samples
Known GenesEYA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615509
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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