A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4156



Internal ID15548837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:187070163..187115390hg38UCSC Ensembl
Outerchr3:186787951..186833178hg19UCSC Ensembl
Outerchr3:188270645..188315872hg18UCSC Ensembl
Outerchr3:188270653..188315880hg17UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3845228
hg1945228
hg1845228
hg1745228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7905
SamplesNA12156
Known GenesST6GAL1
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)nsv4156
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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