A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9504



Internal ID15539810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:31290397..31317311hg38UCSC Ensembl
Outerchr14:31759603..31786517hg19UCSC Ensembl
Outerchr14:30829354..30856268hg18UCSC Ensembl
Outerchr14:30829354..30856268hg17UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3826915
hg1926915
hg1826915
hg1726915
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7250
Supporting Variants
SamplesNA18507
Known GenesHEATR5A
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)nssv9504
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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