A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424183



Internal ID21081736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135600188..136466331hg38UCSC Ensembl
chr7:135284936..136151079hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38866144
hg19866144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18152377
Samples
Known GenesC7orf73, FAM180A, LUZP6, MTPN, NUP205, SLC13A4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424183
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