A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608209



Internal ID20981280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:13183343..13254627hg38UCSC Ensembl
chr7:13222968..13294252hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3871285
hg1971285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6590n223
Supporting Variantsnssv18150661
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608209
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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