A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv971775



Internal ID16265731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:123448402..123449522hg38UCSC Ensembl
Innerchr3:123167249..123168369hg19UCSC Ensembl
Innerchr3:124649939..124651059hg18UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg381121
hg191121
hg181121
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591412
Supporting Variants
Samples
Known GenesADCY5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv971775
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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