A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606095



Internal ID20979166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:123953916..124079424hg38UCSC Ensembl
chr6:124275061..124400569hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38125509
hg19125509
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138882
Samples
Known GenesNKAIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606095
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