A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2727



Internal ID15541847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:65836542..65862719hg38UCSC Ensembl
Outerchr6:66546435..66572612hg19UCSC Ensembl
Outerchr6:66603156..66629333hg18UCSC Ensembl
Outerchr6:66603156..66629333hg17UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg386199
hg196199
hg186199
hg176199
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5330
Supporting Variants
SamplesNA18555
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)nssv2727
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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