A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037727



Internal ID19126946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:21536424..21619340hg38UCSC Ensembl
Innerchr12:21689358..21772274hg19UCSC Ensembl
Innerchr12:21580625..21663541hg18UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg3882917
hg1982917
hg1882917
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3504246
Samples
Known GenesGYS2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037727
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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