A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18034964



Internal ID20602004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32674497..32675263hg38UCSC Ensembl
chr17:31001515..31002281hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38767
hg19767
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6510130
Supporting Variants
Samples
Known GenesMYO1D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18034964
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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