A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602626



Internal ID20975697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:88361640..88362463hg38UCSC Ensembl
chr7:87990955..87991778hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg38824
hg19824
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161944
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602626
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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