A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9560



Internal ID15193068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:109674297..109713119hg38UCSC Ensembl
Outerchr1:110216919..110255741hg19UCSC Ensembl
Outerchr1:110018442..110057264hg18UCSC Ensembl
Outerchr1:109928961..109967783hg17UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3838823
hg1938823
hg1838823
hg1738823
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2310
Supporting Variants
SamplesNA18507
Known GenesGSTM1, GSTM2, GSTM5
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)nssv9560
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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