A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606



Internal ID15551532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:88633976..88663581hg38UCSC Ensembl
Outerchr9:91248891..91278496hg19UCSC Ensembl
Outerchr9:90438711..90468316hg18UCSC Ensembl
Outerchr9:88478445..88508050hg17UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg385986
hg195986
hg185986
hg175986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8628, nssv3729
SamplesNA12156, NA12878
Known GenesLOC286238
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)nsv6606
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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