A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617378



Internal ID20990449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:19963552..20044827hg38UCSC Ensembl
chr7:20003175..20084450hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3881276
hg1981276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18156847
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617378
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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