A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610985



Internal ID20984056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:96348808..96360432hg38UCSC Ensembl
chr7:95978120..95989744hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3811625
hg1911625
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236955
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610985
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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