A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441929



Internal ID21099482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:102586583..102600827hg38UCSC Ensembl
chr9:105348865..105363109hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3814245
hg1914245
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18174485
Samples
Known GenesLINC00587
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441929
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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