A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7295



Internal ID15205604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:59999780..60151634hg38UCSC Ensembl
Outerchr17:58077141..58228995hg19UCSC Ensembl
Outerchr17:55431923..55583777hg18UCSC Ensembl
Outerchr17:55431923..55583777hg17UCSC Ensembl
Cytoband17q23.1
Allele length
AssemblyAllele length
hg38151855
hg19151855
hg18151855
hg17151855
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5665, nssv5666
SamplesNA19129
Known GenesCA4, HEATR6, LOC645638, LOC653653, MIR4737, TBC1D3P1-DHX40P1
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)nsv7295
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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