A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv967



Internal ID15544810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:122590228..122637151hg38UCSC Ensembl
Outerchr10:124349744..124396667hg19UCSC Ensembl
Outerchr10:124339734..124386657hg18UCSC Ensembl
Outerchr10:124339734..124386657hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3846924
hg1946924
hg1846924
hg1746924
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7581
Supporting Variants
SamplesNA19240
Known GenesDMBT1
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)nssv967
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