A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039601



Internal ID19128820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:84532545..84590816hg38UCSC Ensembl
Innerchr12:84926324..84984595hg19UCSC Ensembl
Innerchr12:83450455..83508726hg18UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg3858272
hg1958272
hg1858272
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3524753
Samples
Known GenesMIR548T
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039601
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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