A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407436



Internal ID21064989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:26053336..26086579hg38UCSC Ensembl
chr6:26053564..26086807hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3833244
hg1933244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140724
Samples
Known GenesHIST1H1C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407436
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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