A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325665



Internal ID20858796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:179456420..179462243hg38UCSC Ensembl
chr1:179425555..179431378hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg385824
hg195824
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18054136
Samples
Known GenesAXDND1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325665
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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