A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046758



Internal ID19135977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:94235844..94285021hg38UCSC Ensembl
Innerchr15:94779073..94828250hg19UCSC Ensembl
Innerchr15:92580077..92629254hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3849178
hg1949178
hg1849178
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2665n100
Supporting Variantsnssv3555277, nssv3555273, nssv3555274, nssv3555272, nssv3718211, nssv3555278, nssv3555276, nssv3555275, nssv3718212, nssv3555271
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046758
Frequency
Sample Size11257
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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