A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614099



Internal ID20987170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73808910..73808966hg38UCSC Ensembl
chr7:73223240..73223296hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18159483
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614099
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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