A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055119



Internal ID18797650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:50569273..50608488hg38UCSC Ensembl
Innerchr15:50861470..50900685hg19UCSC Ensembl
Innerchr15:48648762..48687977hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3839216
hg1939216
hg1839216
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552393
Samples
Known GenesTRPM7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055119
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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