A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611051



Internal ID20984122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:4638480..4641746hg38UCSC Ensembl
chr7:4678111..4681377hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg383267
hg193267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155349
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611051
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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