A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608528



Internal ID20981599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97694653..97721640hg38UCSC Ensembl
chr7:97323965..97350952hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3826988
hg1926988
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235040
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608528
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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