A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7636



Internal ID15205979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:960197..981120hg38UCSC Ensembl
Outerchr11:960197..981120hg19UCSC Ensembl
Outerchr11:950197..971120hg18UCSC Ensembl
Outerchr11:950197..971120hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg387840
hg197840
hg187840
hg177840
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6430, nssv5334
SamplesNA19129, NA12156
Known GenesAP2A2
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)nsv7636
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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