A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317252



Internal ID20850336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:14989301..14992500hg38UCSC Ensembl
chr1:15315797..15318996hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052927
Samples
Known GenesKAZN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317252
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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