A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603659



Internal ID20976730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:101928401..101939900hg38UCSC Ensembl
chr7:101571681..101583180hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3811500
hg1911500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18151233
Samples
Known GenesCUX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603659
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