A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420762



Internal ID21078315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:130730645..130731387hg38UCSC Ensembl
chr7:130415473..130416215hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg38743
hg19743
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153466
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420762
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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