A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974476



Internal ID18609687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:83967278..83974868hg38UCSC Ensembl
Innerchr14:84433622..84441212hg19UCSC Ensembl
Innerchr14:83503375..83510965hg18UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg387591
hg197591
hg187591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2758819
SamplesHGDP01284
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974476
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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