A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041702



Internal ID18784233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30376250..30488448hg38UCSC Ensembl
Innerchr15:30668453..30780651hg19UCSC Ensembl
Innerchr15:28455745..28567943hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38112199
hg19112199
hg18112199
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2521n100
Supporting Variantsnssv3547552, nssv3547554, nssv3547555, nssv3547553, nssv3547557, nssv3547550, nssv3547556, nssv3547551, nssv3547558
Samples
Known GenesCHRFAM7A, LOC101059918
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041702
Frequency
Sample Size29084
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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