A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv789968



Internal ID15737238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:27762012..27780963hg38UCSC Ensembl
Innerchr12:27914945..27933896hg19UCSC Ensembl
Innerchr12:27806212..27825163hg18UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg3818952
hg1918952
hg1818952
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv557824
Supporting Variants
Samples
Known GenesKLHL42, MANSC4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv789968
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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