A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617519



Internal ID20990590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:127287884..127288084hg38UCSC Ensembl
chr6:127609029..127609229hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg38201
hg19201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137664
Samples
Known GenesRNF146
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617519
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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