A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318462



Internal ID20851554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:14861147..14866455hg38UCSC Ensembl
chr1:15187643..15192951hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg385309
hg195309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052898
Samples
Known GenesKAZN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318462
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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