A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971



Internal ID15206306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:26754178..26799901hg38UCSC Ensembl
Outerchr13:27328315..27374038hg19UCSC Ensembl
Outerchr13:26226315..26272038hg18UCSC Ensembl
Outerchr13:26226315..26272038hg17UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3845724
hg1945724
hg1845724
hg1745724
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6552
SamplesNA12156
Known GenesGPR12
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)nsv971
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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