A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18201542



Internal ID20768583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16850901..16974000hg38UCSC Ensembl
chr1:17177396..17300495hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38123100
hg19123100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6333329
Supporting Variants
Samples
Known GenesCROCC, MIR3675
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18201542
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.46909


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer