A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334527



Internal ID20867714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:215017201..215018500hg38UCSC Ensembl
chr1:215190544..215191843hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057873
Samples
Known GenesKCNK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334527
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