A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6406



Internal ID15190772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:88797991..88829279hg38UCSC Ensembl
Outerchr10:90557748..90589036hg19UCSC Ensembl
Outerchr10:90547728..90579016hg18UCSC Ensembl
Outerchr10:90547728..90579016hg17UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg388150
hg198150
hg188150
hg178150
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7484
Supporting Variants
SamplesNA12156
Known GenesANKRD22, LIPM
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)nssv6406
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