A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7523



Internal ID8519523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:26741698..26786540hg38UCSC Ensembl
Outerchr1:27068189..27113031hg19UCSC Ensembl
Outerchr1:26940776..26985618hg18UCSC Ensembl
Outerchr1:26752331..26797173hg17UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3844843
hg1944843
hg1844843
hg1744843
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8873
SamplesNA12156
Known GenesARID1A
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)nsv7523
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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