A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7135n223



Internal ID22810103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141577801..141584200hg38UCSC Ensembl
chr7:141277601..141284000hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg386400
hg196400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6429267, nsv6428171
Samples
Known GenesAGK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7135n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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