A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605901



Internal ID20978972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:118045250..118056888hg38UCSC Ensembl
chr6:118366413..118378051hg19UCSC Ensembl
Cytoband6q22.2
Allele length
AssemblyAllele length
hg3811639
hg1911639
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137314
Samples
Known GenesSLC35F1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605901
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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