A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335463



Internal ID20868655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15576552..15607852hg38UCSC Ensembl
chr1:15903047..15934347hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3831301
hg1931301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052091
Samples
Known GenesAGMAT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335463
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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