A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563



Internal ID15551485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:73700670..73743540hg38UCSC Ensembl
Outerchr9:76315586..76358456hg19UCSC Ensembl
Outerchr9:75505406..75548276hg18UCSC Ensembl
Outerchr9:73545140..73588010hg17UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg386171
hg196171
hg186171
hg176171
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8611, nssv1787
SamplesNA12156, NA18555
Known Genes
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)nsv6563
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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