A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049975



Internal ID18792506
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 StatusM
Merged Variants
Supporting Variantsnssv3542762
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)nsv1049975
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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