A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18034207



Internal ID20601247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:12701601..12702800hg38UCSC Ensembl
chr17:12604918..12606117hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6507407
Supporting Variants
Samples
Known GenesLOC101928418, MYOCD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18034207
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00128


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