A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436156



Internal ID21093709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128794390..128795452hg38UCSC Ensembl
chr9:131556669..131557731hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg381063
hg191063
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176913
Samples
Known GenesTBC1D13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436156
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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