A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396637



Internal ID21054190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73126670..73128254hg38UCSC Ensembl
chr6:73836393..73837977hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg381585
hg191585
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18147472
Samples
Known GenesKCNQ5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396637
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