A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608210



Internal ID20981281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:36385601..36394100hg38UCSC Ensembl
chr7:36425210..36433709hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg388500
hg198500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226337
Samples
Known GenesANLN, KIAA0895
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608210
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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