A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506069



Internal ID20879344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:12699908..12700411hg38UCSC Ensembl
chr17:12603225..12603728hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38504
hg19504
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034206
Samples
Known GenesLOC101928418, MYOCD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506069
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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