A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045992



Internal ID18788523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30304080..30488448hg38UCSC Ensembl
Innerchr15:30596283..30780651hg19UCSC Ensembl
Innerchr15:28383575..28567943hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38184369
hg19184369
hg18184369
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2513n100
Supporting Variantsnssv3546740
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)nsv1045992
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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