A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612094



Internal ID20985165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:138971290..138972007hg38UCSC Ensembl
chr6:139292427..139293144hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38718
hg19718
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138412
Samples
Known GenesREPS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612094
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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