A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572



Internal ID15551495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:77044544..77071418hg38UCSC Ensembl
Outerchr9:79659460..79686334hg19UCSC Ensembl
Outerchr9:78849280..78876154hg18UCSC Ensembl
Outerchr9:76889014..76915888hg17UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3812875
hg1912875
hg1812875
hg1712875
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3726
SamplesNA12878
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)nsv6572
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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