A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436895



Internal ID21094448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97696371..97840954hg38UCSC Ensembl
chr9:100458653..100603236hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38144584
hg19144584
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229382
Samples
Known GenesXPA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436895
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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