A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232606



Internal ID20799646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:8903948..10890223hg38UCSC Ensembl
chr7:8943578..10929850hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg381986276
hg191986273
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6607308
Supporting Variants
Samples
Known GenesPER4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232606
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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