A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610131



Internal ID20983202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:95310618..95311094hg38UCSC Ensembl
chr7:94939930..94940406hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38477
hg19477
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161619
Samples
Known GenesPON1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610131
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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