A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052725



Internal ID19141944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7803647..8056051hg38UCSC Ensembl
Innerchr16:7853649..8106053hg19UCSC Ensembl
Innerchr16:7793650..8046054hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38252405
hg19252405
hg18252405
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2720n100
Supporting Variantsnssv3557092
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052725
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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