A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429550



Internal ID21087103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:131596905..131607224hg38UCSC Ensembl
chr7:131281664..131291983hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3810320
hg1910320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154115
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429550
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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