A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7201



Internal ID15552187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:37061793..37149088hg38UCSC Ensembl
Outerchr10:37350721..37438016hg19UCSC Ensembl
Outerchr10:37390727..37478022hg18UCSC Ensembl
Outerchr10:37390727..37478022hg17UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3887296
hg1987296
hg1887296
hg1787296
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv11238, nssv827, nssv1890, nssv836
SamplesNA15510, NA18555, NA19240
Known GenesANKRD30A
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)nsv7201
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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