A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4165



Internal ID15202161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:204984504..205016602hg38UCSC Ensembl
Outerchr1:204953632..204985730hg19UCSC Ensembl
Outerchr1:203220255..203252353hg18UCSC Ensembl
Outerchr1:201685289..201717387hg17UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg387406
hg197406
hg187406
hg177406
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10450
SamplesNA18956
Known GenesNFASC
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)nsv4165
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