A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148715



Internal ID15855919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104687768..104742230hg38UCSC Ensembl
Innerchr14:105154105..105208567hg19UCSC Ensembl
Innerchr14:104225150..104279612hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3854463
hg1954463
hg1854463
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv566061
Supporting Variants
Samples1798860108_A
Known GenesADSSL1, INF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148715
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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