A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335314



Internal ID20868506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9397008..9459851hg38UCSC Ensembl
chr1:9457067..9519910hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3862844
hg1962844
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203190
Samples
Known GenesLOC100506022
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335314
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