A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415157



Internal ID21072710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:65199201..65200700hg38UCSC Ensembl
chr5:64495028..64496527hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18134396
Samples
Known GenesADAMTS6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415157
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