A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611919



Internal ID20984990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107193257..107193689hg38UCSC Ensembl
chr7:106833702..106834134hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38433
hg19433
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18146942
Samples
Known GenesHBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611919
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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