A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17385281



Internal ID22443151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42467487..42468721hg38UCSC Ensembl
chr15:42759685..42760919hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381235
hg191235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5932003
Supporting Variants
Samples
Known GenesZNF106
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17385281
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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