A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450090



Internal ID21107643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133817401..133818113hg38UCSC Ensembl
chr9:136682523..136683235hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38713
hg19713
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18175216
Samples
Known GenesVAV2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450090
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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