A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499274



Internal ID20872492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:19540779..19555461hg38UCSC Ensembl
chr17:19444092..19458774hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3814683
hg1914683
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034801
Samples
Known GenesSLC47A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499274
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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