A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3526080



Internal ID18824361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:119041241..119062172hg38UCSC Ensembl
Innerchr12:119479046..119499977hg19UCSC Ensembl
Innerchr12:117963429..117984360hg18UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg3820932
hg1920932
hg1820932
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050420
Supporting Variants
Samples
Known GenesSRRM4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3526080
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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