A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv901



Internal ID15198502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:46278445..46292622hg38UCSC Ensembl
Outerchr10:47649681..47663858hg19UCSC Ensembl
Outerchr10:47119687..47133864hg18UCSC Ensembl
Outerchr10:47119687..47133864hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg387016
hg197016
hg187016
hg177016
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6543
Supporting Variants
SamplesNA19240
Known GenesANTXRL
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)nssv901
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