A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610744



Internal ID20983815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:143133401..143136400hg38UCSC Ensembl
chr6:143454538..143457537hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140206
Samples
Known GenesAIG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610744
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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