A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049980



Internal ID19139199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:67241206..67285222hg38UCSC Ensembl
Innerchr15:67533544..67577560hg19UCSC Ensembl
Innerchr15:65320598..65364614hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3844017
hg1944017
hg1844017
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3553650
Samples
Known GenesAAGAB, IQCH
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049980
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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