A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6096555



Internal ID22005788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:136352251..136352251hg38UCSC Ensembl
chr9:139246703..139246703hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597371
Samples
Known GenesGPSM1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6096555
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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