A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614002



Internal ID20987073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23439439..23444623hg38UCSC Ensembl
chr7:23479058..23484242hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg385185
hg195185
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221245
Samples
Known GenesIGF2BP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614002
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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