A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3718223



Internal ID18669818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101112625..101319838hg38UCSC Ensembl
Innerchr15:101652830..101860043hg19UCSC Ensembl
Innerchr15:99470353..99677566hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38207214
hg19207214
hg18207214
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035599
Supporting Variants
Samples
Known GenesCHSY1, LOC100507472, PCSK6, SNRPA1, VIMP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3718223
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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