A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318177



Internal ID20851268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37748124..37754156hg38UCSC Ensembl
chr1:38213796..38219828hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg386033
hg196033
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061210
Samples
Known GenesEPHA10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318177
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