A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613830



Internal ID20986901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:81556932..81557440hg38UCSC Ensembl
chr7:81186248..81186756hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38509
hg19509
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18160914
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613830
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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