A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3482



Internal ID15538210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:157773116..157778480hg38UCSC Ensembl
Outerchr6:158194148..158199512hg19UCSC Ensembl
Outerchr6:158114136..158119500hg18UCSC Ensembl
Outerchr6:158164557..158169921hg17UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg385737
hg195737
hg185737
hg175737
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557
Supporting Variants
SamplesNA12878
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)nssv3482
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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