A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3604396



Internal ID18555991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:107746970..108629120hg38UCSC Ensembl
Innerchr3:107465817..108347967hg19UCSC Ensembl
Innerchr3:108948507..109830657hg18UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg38882151
hg19882151
hg18882151
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011158
Supporting Variants
Samples
Known GenesBBX, CD47, DZIP3, HHLA2, IFT57, KIAA1524, LINC00635, LINC00636, MYH15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3604396
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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