A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3721660



Internal ID18673255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32612402..34538731hg38UCSC Ensembl
Innerchr15:32904603..34830932hg19UCSC Ensembl
Innerchr15:30691895..32618224hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg381926330
hg191926330
hg181926330
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052620
Supporting Variants
Samples
Known GenesARHGAP11A, AVEN, CHRM5, EMC4, EMC7, FMN1, GOLGA8A, GOLGA8B, GREM1, KATNBL1, LOC100131315, LPCAT4, MIR1233-1, MIR1233-2, NOP10, NUTM1, PGBD4, RYR3, SCG5, SLC12A6, TMCO5B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3721660
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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