A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6025



Internal ID15191153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:184829536..184865442hg38UCSC Ensembl
Outerchr1:184798670..184834576hg19UCSC Ensembl
Outerchr1:183065293..183101199hg18UCSC Ensembl
Outerchr1:181530327..181566233hg17UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg3835907
hg1935907
hg1835907
hg1735907
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3843
Supporting Variants
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)nssv6025
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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