A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6618731



Internal ID20991802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:78760587..79463170hg38UCSC Ensembl
chr7:78389903..79092486hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38702584
hg19702584
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234181
Samples
Known GenesMAGI2, MAGI2-AS2, MAGI2-AS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6618731
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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