A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3641112



Internal ID18939393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:135897571..136242073hg38UCSC Ensembl
Innerchr4:136818726..137163228hg19UCSC Ensembl
Innerchr4:137038176..137382678hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38344503
hg19344503
hg18344503
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1025736
Supporting Variants
Samples
Known GenesLINC00613
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3641112
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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