A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402444



Internal ID21059997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:83223723..83226789hg38UCSC Ensembl
chr6:83933442..83936508hg19UCSC Ensembl
Cytoband6q14.2
Allele length
AssemblyAllele length
hg383067
hg193067
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18145328
Samples
Known GenesME1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6402444
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