A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9025



Internal ID15534839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:45280344..45325076hg38UCSC Ensembl
Outerchr12:45674127..45718859hg19UCSC Ensembl
Outerchr12:43960394..44005126hg18UCSC Ensembl
Outerchr12:43960394..44005126hg17UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg3844733
hg1944733
hg1844733
hg1744733
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv690
Supporting Variants
SamplesNA12156
Known GenesANO6
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)nssv9025
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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