A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619428



Internal ID20992499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:36363101..36371400hg38UCSC Ensembl
chr7:36402710..36411009hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg388300
hg198300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231589
Samples
Known GenesKIAA0895
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619428
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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