A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6050



Internal ID15537814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:6941075..6973503hg38UCSC Ensembl
Outerchr6:6941308..6973736hg19UCSC Ensembl
Outerchr6:6886307..6918735hg18UCSC Ensembl
Outerchr6:6886307..6918735hg17UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg387011
hg197011
hg187011
hg177011
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5185
Supporting Variants
SamplesNA12156
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)nssv6050
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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