A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3742866



Internal ID18694461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:69979953..70947088hg38UCSC Ensembl
Innerchr4:70845671..71812805hg19UCSC Ensembl
Innerchr4:70880260..72031669hg18UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38967136
hg19967135
hg181151410
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012495
Supporting Variants
Samples
Known GenesAMBN, AMTN, C4orf40, CABS1, CSN1S2AP, CSN1S2BP, CSN3, ENAM, FDCSP, GRSF1, HTN1, HTN3, IGJ, MOB1B, MUC7, ODAM, PROL1, RUFY3, SMR3A, SMR3B, STATH, UTP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3742866
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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