A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10675



Internal ID15195437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:91734013..91766363hg38UCSC Ensembl
Outerchr9:94496295..94528645hg19UCSC Ensembl
Outerchr9:93536116..93568466hg18UCSC Ensembl
Outerchr9:91575850..91608200hg17UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg387156
hg197156
hg187156
hg177156
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6613
Supporting Variants
SamplesNA18956
Known GenesROR2
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)nssv10675
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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