A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611825



Internal ID20984896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:25028094..25183195hg38UCSC Ensembl
chr7:25067713..25222814hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38155102
hg19155102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236733
Samples
Known GenesC7orf31, CYCS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611825
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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