A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608619



Internal ID20981690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:81130502..81137019hg38UCSC Ensembl
chr7:80759818..80766335hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg386518
hg196518
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6975n223
Supporting Variantsnssv18160863
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608619
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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