A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326893



Internal ID20860030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15856283..15861346hg38UCSC Ensembl
chr1:16182778..16187841hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg385064
hg195064
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053059
Samples
Known GenesSPEN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326893
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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