A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4923



Internal ID15542915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:76301044..76324573hg38UCSC Ensembl
Outerchr6:77010761..77034290hg19UCSC Ensembl
Outerchr6:77067481..77091010hg18UCSC Ensembl
Outerchr6:77067481..77091010hg17UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3823530
hg1923530
hg1823530
hg1723530
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5357
Supporting Variants
SamplesNA19129
Known Genes
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)nssv4923
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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