A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322126



Internal ID20855236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27479178..27483299hg38UCSC Ensembl
chr1:27805689..27809810hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg384122
hg194122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060670
Samples
Known GenesWASF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322126
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