A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3895



Internal ID15538622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:98926648..98947233hg38UCSC Ensembl
Outerchr10:100686405..100706990hg19UCSC Ensembl
Outerchr10:100676395..100696980hg18UCSC Ensembl
Outerchr10:100676395..100696980hg17UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3820586
hg1920586
hg1820586
hg1720586
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7513
Supporting Variants
SamplesNA12878
Known GenesHPSE2
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)nssv3895
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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