A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611842



Internal ID20984913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75920083..75921331hg38UCSC Ensembl
chr7:75549401..75550649hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg381249
hg191249
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18158775
Samples
Known GenesPOR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611842
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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