A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616



Internal ID15551543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:92752652..92799109hg38UCSC Ensembl
Outerchr9:95514934..95561391hg19UCSC Ensembl
Outerchr9:94554755..94601212hg18UCSC Ensembl
Outerchr9:92594489..92640946hg17UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg386506
hg196506
hg186506
hg176506
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2816, nssv818
SamplesNA18555, NA19240
Known GenesBICD2
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)nsv6616
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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