A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397616



Internal ID21055169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15283221..15290787hg38UCSC Ensembl
chr6:15283452..15291018hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg387567
hg197567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6065n223
Supporting Variantsnssv18141571
Samples
Known GenesJARID2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397616
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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