A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044077



Internal ID18786608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:44895124..44944451hg38UCSC Ensembl
Innerchr13:45469259..45518586hg19UCSC Ensembl
Innerchr13:44367259..44416586hg18UCSC Ensembl
Cytoband13q14.12
Allele length
AssemblyAllele length
hg3849328
hg1949328
hg1849328
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523425
Samples
Known GenesNUFIP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044077
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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