A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3345



Internal ID15201259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:31549053..31593946hg38UCSC Ensembl
Outerchr20:30136856..30181749hg19UCSC Ensembl
Outerchr20:29600517..29645410hg18UCSC Ensembl
Outerchr20:29600517..29645410hg17UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3844894
hg1944894
hg1844894
hg1744894
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7669
SamplesNA12156
Known GenesHM13, HM13-AS1
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)nsv3345
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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