A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619176



Internal ID20992247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87124454..87285053hg38UCSC Ensembl
chr7:86753770..86914369hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg38160600
hg19160600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221511
Samples
Known GenesDMTF1, TMEM243
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619176
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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