A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514605



Internal ID20887960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8293727..8293998hg38UCSC Ensembl
chr17:8197045..8197316hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38272
hg19272
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038353
Samples
Known GenesSLC25A35
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514605
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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