A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446649



Internal ID21104202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:68729201..68730100hg38UCSC Ensembl
chr9:71344117..71345016hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196663
Samples
Known GenesPIP5K1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446649
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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