A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633



Internal ID15203776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:8013996..8020241hg38UCSC Ensembl
Outerchr7:8053626..8059871hg19UCSC Ensembl
Outerchr7:8020151..8026396hg18UCSC Ensembl
Outerchr7:7826866..7833111hg17UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg387205
hg197205
hg187205
hg177205
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv611
SamplesNA19240
Known GenesGLCCI1
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)nsv5633
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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