A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233767



Internal ID20800807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103128147..103167177hg38UCSC Ensembl
chr7:102768594..102807624hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3839031
hg1939031
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610784
Supporting Variants
Samples
Known GenesNAPEPLD, RPL19P12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233767
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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