A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454648



Internal ID21112201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134857571..134858962hg38UCSC Ensembl
chr9:137749417..137750808hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg381392
hg191392
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18175963
Samples
Known GenesLOC101448202
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454648
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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