A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052802



Internal ID18795333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:12672503..12870391hg38UCSC Ensembl
Innerchr16:12766360..12964248hg19UCSC Ensembl
Innerchr16:12673861..12871749hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg38197889
hg19197889
hg18197889
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3557220
Samples
Known GenesCPPED1, MIR4718
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052802
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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