A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv723



Internal ID15552218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:57321090..57352277hg38UCSC Ensembl
Outerchr12:57714873..57746060hg19UCSC Ensembl
Outerchr12:56001140..56032327hg18UCSC Ensembl
Outerchr12:56001140..56032327hg17UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg388305
hg198305
hg188305
hg178305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10866
SamplesNA18956
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)nsv723
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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