A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5156



Internal ID15549937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:178919824..178940066hg38UCSC Ensembl
Outerchr5:178346825..178367067hg19UCSC Ensembl
Outerchr5:178279431..178299673hg18UCSC Ensembl
Outerchr5:178279431..178299673hg17UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3820243
hg1920243
hg1820243
hg1720243
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4881
SamplesNA19129
Known GenesZFP2
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)nsv5156
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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