A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617850



Internal ID20990921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:101462920..101463302hg38UCSC Ensembl
chr6:101910796..101911178hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38383
hg19383
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133893
Samples
Known GenesGRIK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617850
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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