A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404598



Internal ID21062151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:93264501..93318200hg38UCSC Ensembl
chr6:93974219..94027918hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3853700
hg1953700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225288
Samples
Known GenesEPHA7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404598
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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