A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402768



Internal ID21060321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:92944154..92954541hg38UCSC Ensembl
chr6:93653872..93664259hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3810388
hg1910388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18148807
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6402768
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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