A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327283



Internal ID20860420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46661522..46666662hg38UCSC Ensembl
chr1:47127194..47132334hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg385141
hg195141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061574
Samples
Known GenesATPAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327283
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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