A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5773



Internal ID15196950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:109681901..109710798hg38UCSC Ensembl
Outerchr1:110224523..110253420hg19UCSC Ensembl
Outerchr1:110026046..110054943hg18UCSC Ensembl
Outerchr1:109936565..109965462hg17UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3828898
hg1928898
hg1828898
hg1728898
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2310
Supporting Variants
SamplesNA19129
Known GenesGSTM1, GSTM2
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)nssv5773
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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