A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506894



Internal ID20880181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:30235301..30239000hg38UCSC Ensembl
chr17:28562319..28566018hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg383700
hg193700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034742
Samples
Known GenesSLC6A4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506894
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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