A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3525



Internal ID15538253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:47146604..47182082hg38UCSC Ensembl
Outerchr7:47186202..47221680hg19UCSC Ensembl
Outerchr7:47152727..47188205hg18UCSC Ensembl
Outerchr7:46959442..46994920hg17UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg384256
hg194256
hg184256
hg174256
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5728
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)nssv3525
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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