A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503057



Internal ID20876308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39411798..39412816hg38UCSC Ensembl
chr17:37568051..37569069hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381019
hg191019
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035354
Samples
Known GenesMED1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503057
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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