A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170275



Internal ID21314336
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 TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14248859, nssv14243578, nssv14247812, nssv14242658, nssv14240809, nssv14244907, nssv14242202, nssv14246977, nssv14252496
SamplesNGO_12, NGO_10, NGO_9, PML_1, NGO_43, NGO_19, SNI_16, NGO_55, NGO_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)nsv3170275
Frequency
Sample Size93
Observed Gain3
Observed Loss6
Observed Complex0
Frequencyn/a


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