A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322144



Internal ID20855254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:160165529..160166042hg38UCSC Ensembl
chr1:160135319..160135832hg19UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg38514
hg19514
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052447
Samples
Known GenesATP1A4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322144
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