A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406464



Internal ID21064017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73616760..73627780hg38UCSC Ensembl
chr6:74326483..74337503hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3811021
hg1911021
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18147512
Samples
Known GenesSLC17A5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406464
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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