A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455386



Internal ID21112939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130173101..130938500hg38UCSC Ensembl
chr9:132935380..133813887hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38765400
hg19878508
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219770
Samples
Known GenesABL1, ASS1, EXOSC2, FIBCD1, FUBP3, LOC100272217, MIR6856, NCS1, PRDM12, QRFP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455386
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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