A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452614



Internal ID21110167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127901750..127914126hg38UCSC Ensembl
chr9:130664029..130676405hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3812377
hg1912377
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176837
Samples
Known GenesST6GALNAC4, ST6GALNAC6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452614
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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