A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412682



Internal ID21070235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43030686..43031251hg38UCSC Ensembl
chr6:42998424..42998989hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38566
hg19566
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143407
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412682
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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