A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412736



Internal ID21070289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:96199591..96200389hg38UCSC Ensembl
chr6:96647467..96648265hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38799
hg19799
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150440
Samples
Known GenesFUT9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412736
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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