A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10692



Internal ID15542106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:136734576..136752174hg38UCSC Ensembl
Outerchr9:139629028..139646626hg19UCSC Ensembl
Outerchr9:138748849..138766447hg18UCSC Ensembl
Outerchr9:136904865..136922463hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3810175
hg1910175
hg1810175
hg1710175
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6769
Supporting Variants
SamplesNA18956
Known GenesLCN10, LCN6, LOC100128593, MIR6722
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)nssv10692
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