A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076



Internal ID15204263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:22089806..22123911hg38UCSC Ensembl
Outerchr1:22416299..22450404hg19UCSC Ensembl
Outerchr1:22288886..22322991hg18UCSC Ensembl
Outerchr1:22161605..22195710hg17UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg385924
hg195924
hg185924
hg175924
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2871
SamplesNA18555
Known GenesCDC42, WNT4
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)nsv6076
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