A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035599



Internal ID18778130
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 StatusM
Merged Variants
Supporting Variantsnssv3718223
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)nsv1035599
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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