A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100112



Internal ID22009345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:136352335..136352335hg38UCSC Ensembl
chr9:139246787..139246787hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578947
Samples
Known GenesGPSM1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100112
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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