A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv830849



Internal ID6156573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:158539223..158700882hg19UCSC Ensembl
Outerchr6:158459211..158620870hg18UCSC Ensembl
Outerchr6:158509632..158671291hg17UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv1445716, nssv1445715
Samples
Known GenesGTF2H5, SERAC1
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv830849
Frequency
Sample Size95
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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