A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049577



Internal ID18792108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101123620..101501317hg38UCSC Ensembl
Innerchr15:101663825..102041520hg19UCSC Ensembl
Innerchr15:99481348..99859043hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38377698
hg19377696
hg18377696
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3555332
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)nsv1049577
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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