A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615



Internal ID15551542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:92224809..92258551hg38UCSC Ensembl
Outerchr9:94987091..95020833hg19UCSC Ensembl
Outerchr9:94026912..94060654hg18UCSC Ensembl
Outerchr9:92066646..92100388hg17UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg385697
hg195697
hg185697
hg175697
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8633
SamplesNA12156
Known GenesIARS
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)nsv6615
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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