A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9031



Internal ID15534833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:53572319..53582635hg38UCSC Ensembl
Outerchr12:53966103..53976419hg19UCSC Ensembl
Outerchr12:52252370..52262686hg18UCSC Ensembl
Outerchr12:52252370..52262686hg17UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg3810317
hg1910317
hg1810317
hg1710317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv715
Supporting Variants
SamplesNA12156
Known GenesATF7
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)nssv9031
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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