A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602129



Internal ID20975200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:113535201..113539900hg38UCSC Ensembl
chr7:113175256..113179955hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg384700
hg194700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228714
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602129
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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