A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327775



Internal ID20860917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:61839802..61873620hg38UCSC Ensembl
chr1:62305474..62339292hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3833819
hg1933819
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203652
Samples
Known GenesINADL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327775
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