A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5778



Internal ID15550621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:67690700..67712028hg38UCSC Ensembl
Outerchr7:67155687..67177015hg19UCSC Ensembl
Outerchr7:66793122..66814450hg18UCSC Ensembl
Outerchr7:66599837..66621165hg17UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg385965
hg195965
hg185965
hg175965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2764
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)nsv5778
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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