A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436413



Internal ID21093966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112136043..112138262hg38UCSC Ensembl
chr9:114898323..114900542hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg382220
hg192220
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18175238
Samples
Known GenesMIR3134, SUSD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436413
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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