A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332110



Internal ID20865279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:52037201..52040600hg38UCSC Ensembl
chr1:52502873..52506272hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg383400
hg193400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062022
Samples
Known GenesTXNDC12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332110
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