A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409672



Internal ID21067225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31813065..31824411hg38UCSC Ensembl
chr6:31780842..31792188hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3811347
hg1911347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18142129
Samples
Known GenesHSPA1A, HSPA1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409672
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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