A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608759



Internal ID20981830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:102239793..102240923hg38UCSC Ensembl
chr7:101883073..101884203hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg381131
hg191131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18151251
Samples
Known GenesCUX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608759
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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