A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609713



Internal ID20982784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:82890593..82891651hg38UCSC Ensembl
chr7:82519909..82520967hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg381059
hg191059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18160394
Samples
Known GenesPCLO
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609713
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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