A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322243



Internal ID20855354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35291947..35293171hg38UCSC Ensembl
chr1:35757548..35758772hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg381225
hg191225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061056
Samples
Known GenesZMYM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322243
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