A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14242658



Internal ID21307669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32166460..32535335hg38UCSC Ensembl
Outerchr15:32151995..32550921hg38UCSC Ensembl
Innerchr15:32458661..32827536hg19UCSC Ensembl
Outerchr15:32444196..32843122hg19UCSC Ensembl
Innerchr15:30245953..30614828hg18UCSC Ensembl
Outerchr15:30231488..30630414hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38398927
hg19398927
hg18398927
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170275
Supporting Variants
SamplesNGO_36
Known GenesCHRNA7, GOLGA8K, GOLGA8O, LOC100996255, ULK4P1, ULK4P2, ULK4P3, WHAMMP1
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14242658
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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