A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039906



Internal ID18782437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:41184011..41226778hg38UCSC Ensembl
Innerchr15:41476209..41518976hg19UCSC Ensembl
Innerchr15:39263501..39306268hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3842768
hg1942768
hg1842768
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552253
Samples
Known GenesEXD1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039906
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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