A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476723



Internal ID21134276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:29591851..29594783hg38UCSC Ensembl
chr13:30165988..30168920hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg382933
hg192933
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007860
Samples
Known GenesSLC7A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476723
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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