A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3542762



Internal ID18494357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:18564935..18768126hg38UCSC Ensembl
Innerchr16:18576257..18779448hg19UCSC Ensembl
Innerchr16:18483758..18686949hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38203192
hg19203192
hg18203192
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049975
Supporting Variants
Samples
Known GenesABCC6P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3542762
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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