A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155375



Internal ID22085880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:11985188..12011145hg38UCSC Ensembl
Outerchr17:11979403..12015324hg38UCSC Ensembl
Innerchr17:11888505..11914462hg19UCSC Ensembl
Outerchr17:11882720..11918641hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3835922
hg1935922
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4010084
Samples
Known GenesZNF18
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155375
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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