A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1355



Internal ID15199232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:74834571..74880707hg38UCSC Ensembl
Outerchr14:75301274..75347410hg19UCSC Ensembl
Outerchr14:74371027..74417163hg18UCSC Ensembl
Outerchr14:74371027..74417163hg17UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3846137
hg1946137
hg1846137
hg1746137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6601
SamplesNA12156
Known GenesPROX2, YLPM1
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)nsv1355
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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