A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004663



Internal ID21914006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:78505883..78505934hg38UCSC Ensembl
chr7:78135200..78135251hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17571928
Samples
Known GenesMAGI2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004663
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer