A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045761



Internal ID18788292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84192647..84554155hg38UCSC Ensembl
Innerchr15:84861399..85097386hg19UCSC Ensembl
Innerchr15:82652403..82898390hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38361509
hg19235988
hg18245988
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2642n100
Supporting Variantsnssv3555049, nssv3718127, nssv3718124, nssv3555050, nssv3718126, nssv3718125
Samples
Known GenesDNM1P41, GOLGA6L4, GOLGA6L5P, LOC388152, LOC440300, LOC642423, UBE2Q2P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045761
Frequency
Sample Size29084
Observed Gain5
Observed Loss1
Observed Complex0
Frequencyn/a


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