A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6684



Internal ID15551618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:115950121..115983651hg38UCSC Ensembl
Outerchr9:118712400..118745930hg19UCSC Ensembl
Outerchr9:117752221..117785751hg18UCSC Ensembl
Outerchr9:115791954..115825484hg17UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg385906
hg195906
hg185906
hg175906
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8657
SamplesNA12156
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)nsv6684
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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