A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615540



Internal ID20988611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:47606353..47618379hg38UCSC Ensembl
chr7:47645951..47657977hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3812027
hg1912027
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155437
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615540
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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