A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497529



Internal ID20870736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15466963..15513680hg38UCSC Ensembl
chr17:15370277..15416994hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3846718
hg1946718
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183411
Samples
Known GenesCDRT4, TVP23C, TVP23C-CDRT4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497529
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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