A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051581



Internal ID19140800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:82362975..82585560hg38UCSC Ensembl
Innerchr14:82829319..83051904hg19UCSC Ensembl
Innerchr14:81899072..82121657hg18UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38222586
hg19222586
hg18222586
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531231
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051581
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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