A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038151



Internal ID18780682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:15165037..15407242hg38UCSC Ensembl
Innerchr16:15258894..15501099hg19UCSC Ensembl
Innerchr16:15166395..15408600hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38242206
hg19242206
hg18242206
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3718983
Samples
Known GenesMPV17L, NPIPA5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038151
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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