A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612617



Internal ID20985688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:146040633..146041085hg38UCSC Ensembl
chr6:146361769..146362221hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg38453
hg19453
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139004
Samples
Known GenesGRM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612617
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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