A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052620



Internal ID18795151
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 StatusM
Merged Variants
Supporting Variantsnssv3721660
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)nsv1052620
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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