A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617362



Internal ID20990433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:101583558..101584087hg38UCSC Ensembl
chr6:102031433..102031962hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38530
hg19530
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18134534
Samples
Known GenesGRIK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617362
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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