A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401332



Internal ID21058885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2229661..2263894hg38UCSC Ensembl
chr6:2229895..2264128hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3834234
hg1934234
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232214
Samples
Known GenesGMDS, GMDS-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401332
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer