A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320785



Internal ID20853886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16004447..16008525hg38UCSC Ensembl
chr1:16330942..16335020hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg384079
hg194079
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052441
Samples
Known GenesC1orf64
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320785
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer