A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611413



Internal ID20984484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103134521..103136136hg38UCSC Ensembl
chr7:102774968..102776583hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg381616
hg191616
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222355
Samples
Known GenesNAPEPLD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611413
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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