A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410990



Internal ID21068543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42160965..42162190hg38UCSC Ensembl
chr6:42128703..42129928hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg381226
hg191226
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143362
Samples
Known GenesGUCA1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410990
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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