A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497298



Internal ID20870504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38534458..38536678hg38UCSC Ensembl
chr17:36690693..36692913hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg382221
hg192221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035284
Samples
Known GenesSRCIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497298
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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