A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617693



Internal ID20990764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20092223..20104629hg38UCSC Ensembl
chr7:20131846..20144252hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3812407
hg1912407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18156867
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617693
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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