A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411224



Internal ID21068777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:93398901..93440400hg38UCSC Ensembl
chr6:94108619..94150118hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3841500
hg1941500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220072
Samples
Known GenesEPHA7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411224
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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