A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316638



Internal ID20849718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:178327111..178328086hg38UCSC Ensembl
chr1:178296246..178297221hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg38976
hg19976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18054045
Samples
Known GenesRASAL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316638
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