A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430990



Internal ID21088543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135593401..135594400hg38UCSC Ensembl
chr7:135278149..135279148hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18152376
Samples
Known GenesNUP205
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430990
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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