A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17365722



Internal ID22591391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15160438..15164966hg38UCSC Ensembl
chr1:15486934..15491462hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg384529
hg194529
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5875535
Supporting Variants
Samples
Known GenesC1orf195, TMEM51
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17365722
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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