A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613



Internal ID15204854
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 StatusM
Merged Variants
Supporting Variantsnssv10675
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)nsv6613
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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