A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617613



Internal ID20990684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:84511201..84518000hg38UCSC Ensembl
chr7:84140517..84147316hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg386800
hg196800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161037
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617613
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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