A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10656



Internal ID15542142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:15651854..15683003hg38UCSC Ensembl
Outerchr9:15651852..15683001hg19UCSC Ensembl
Outerchr9:15641852..15673001hg18UCSC Ensembl
Outerchr9:15641852..15673001hg17UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg388349
hg198349
hg188349
hg178349
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6485
Supporting Variants
SamplesNA18956
Known GenesCCDC171
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)nssv10656
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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