A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396623



Internal ID21054176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:96032087..96032634hg38UCSC Ensembl
chr6:96479963..96480510hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38548
hg19548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149861
Samples
Known GenesFUT9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396623
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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