A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6600879



Internal ID20973950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160507360..160661249hg38UCSC Ensembl
chr6:160928392..161082281hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38153890
hg19153890
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216731
Samples
Known GenesLPA, LPAL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6600879
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