A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3832



Internal ID15201795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:184815308..184823537hg38UCSC Ensembl
Outerchr1:184784442..184792671hg19UCSC Ensembl
Outerchr1:183051065..183059294hg18UCSC Ensembl
Outerchr1:181516099..181524328hg17UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg388230
hg198230
hg188230
hg178230
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6014
SamplesNA12156
Known GenesFAM129A
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)nsv3832
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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