A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613596



Internal ID20986667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:72918921..72923986hg38UCSC Ensembl
chr7:72389458..72394523hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg385066
hg195066
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18159428
Samples
Known GenesPOM121
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613596
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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