A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4011843



Internal ID22073474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46554684..46687628hg38UCSC Ensembl
Outerchr17:46494937..46707286hg38UCSC Ensembl
Innerchr17:44632050..44764994hg19UCSC Ensembl
Outerchr17:44572303..44784652hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38212350
hg19212350
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155475
Supporting Variants
Samples
Known GenesARL17A, LRRC37A2, NSF, NSFP1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4011843
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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