A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473229



Internal ID21130782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102530497..102532267hg38UCSC Ensembl
chr11:102401228..102402998hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg381771
hg191771
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195857
Samples
Known GenesMMP7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473229
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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