A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595



Internal ID15551520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:86157864..86170981hg38UCSC Ensembl
Outerchr9:88772779..88785896hg19UCSC Ensembl
Outerchr9:87962599..87975716hg18UCSC Ensembl
Outerchr9:86002333..86015450hg17UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg386550
hg196550
hg186550
hg176550
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2814
SamplesNA18555
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)nsv6595
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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