A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610784



Internal ID20983855
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 StatusM
Merged Variants
Supporting Variantsnssv18233767
Samples
Known GenesNAPEPLD, RPL19P12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610784
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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