A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9965



Internal ID15193373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:84047953..84067615hg38UCSC Ensembl
Outerchr1:84513636..84533298hg19UCSC Ensembl
Outerchr1:84286224..84305886hg18UCSC Ensembl
Outerchr1:84225657..84245319hg17UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3819663
hg1919663
hg1819663
hg1719663
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1732
Supporting Variants
SamplesNA18507
Known Genes
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)nssv9965
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