A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9225



Internal ID15534639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:84021203..84065893hg38UCSC Ensembl
Outerchr14:84487547..84532237hg19UCSC Ensembl
Outerchr14:83557300..83601990hg18UCSC Ensembl
Outerchr14:83557300..83601990hg17UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg3844691
hg1944691
hg1844691
hg1744691
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1382
Supporting Variants
SamplesNA12156
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv9225
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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