A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497900



Internal ID20871108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:37607774..37608658hg38UCSC Ensembl
chr17:35967820..35968706hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38885
hg19887
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035240
Samples
Known GenesSYNRG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497900
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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