A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044435



Internal ID18786966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43883905..44215205hg38UCSC Ensembl
Innerchr15:44176103..44507403hg19UCSC Ensembl
Innerchr15:41963395..42294695hg18UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38331301
hg19331301
hg18331301
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552334
Samples
Known GenesFRMD5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044435
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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