A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11238



Internal ID15539341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:37108180..37148934hg38UCSC Ensembl
Outerchr10:37397108..37437862hg19UCSC Ensembl
Outerchr10:37437114..37477868hg18UCSC Ensembl
Outerchr10:37437114..37477868hg17UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3840755
hg1940755
hg1840755
hg1740755
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7201
Supporting Variants
SamplesNA15510
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)nssv11238
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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