A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10748



Internal ID15195364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:33214316..33246294hg38UCSC Ensembl
Outerchr10:33503244..33535222hg19UCSC Ensembl
Outerchr10:33543250..33575228hg18UCSC Ensembl
Outerchr10:33543250..33575228hg17UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg387522
hg197522
hg187522
hg177522
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6299
Supporting Variants
SamplesNA18956
Known GenesNRP1
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)nssv10748
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer