A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437871



Internal ID21095424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129017631..129018538hg38UCSC Ensembl
chr9:131779910..131780817hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38908
hg19908
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18175180
Samples
Known GenesSH3GLB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437871
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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