A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983968



Internal ID18619159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:23773049..23783850hg38UCSC Ensembl
Innerchr14:24242258..24253059hg19UCSC Ensembl
Innerchr14:23312098..23322899hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3810802
hg1910802
hg1810802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2758263
SamplesHGDP00456
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv983968
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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