A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10968



Internal ID15192870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:109681375..109710259hg38UCSC Ensembl
Outerchr1:110223997..110252881hg19UCSC Ensembl
Outerchr1:110025520..110054404hg18UCSC Ensembl
Outerchr1:109936039..109964923hg17UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3828885
hg1928885
hg1828885
hg1728885
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2310
Supporting Variants
SamplesNA15510
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)nssv10968
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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