A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432531



Internal ID21090084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:2464648..2727898hg38UCSC Ensembl
chr9:2464648..2727898hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38263251
hg19263251
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223623
Samples
Known GenesFLJ35024, KCNV2, VLDLR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432531
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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