A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454649



Internal ID21112202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112208314..112210461hg38UCSC Ensembl
chr9:114970594..114972741hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg382148
hg192148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18175244
Samples
Known GenesMIR3134
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454649
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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