A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560580



Internal ID16001303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:124540561..124541865hg38UCSC Ensembl
Innerchr12:125025107..125026411hg19UCSC Ensembl
Innerchr12:123591060..123592364hg18UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg381305
hg191305
hg181305
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2942n54
Supporting Variantsnssv804123, nssv804122, nssv804125, nssv804124, nssv804121, nssv804120, nssv804119
Samples
Known GenesNCOR2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560580
Frequency
Sample Size17421
Observed Gain5
Observed Loss2
Observed Complex0
Frequencyn/a


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