A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603588



Internal ID20976659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:78728524..78728864hg38UCSC Ensembl
chr7:78357840..78358180hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18158950
Samples
Known GenesMAGI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603588
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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