A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv792631



Internal ID16086587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:33371147..34551070hg38UCSC Ensembl
Innerchr12:33524082..34704005hg19UCSC Ensembl
Innerchr12:33415349..34595272hg18UCSC Ensembl
Cytoband12p11.1
Allele length
AssemblyAllele length
hg381179924
hg191179924
hg181179924
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv558251
Supporting Variants
Samples
Known GenesALG10, SYT10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv792631
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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