A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396658



Internal ID21054211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34441314..34451515hg38UCSC Ensembl
chr6:34409091..34419292hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3810202
hg1910202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141662
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396658
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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