A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7887



Internal ID15535977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:159774699..159795462hg38UCSC Ensembl
Outerchr3:159492488..159513251hg19UCSC Ensembl
Outerchr3:160975182..160995945hg18UCSC Ensembl
Outerchr3:160975190..160995953hg17UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg3820764
hg1920764
hg1820764
hg1720764
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4084
Supporting Variants
SamplesNA12156
Known GenesIQCJ-SCHIP1, SCHIP1
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)nssv7887
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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