A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3557



Internal ID15538285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:98755655..98795168hg38UCSC Ensembl
Outerchr7:98384988..98392791hg19UCSC Ensembl
Outerchr7:98222924..98230727hg18UCSC Ensembl
Outerchr7:98029639..98037442hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3830878
hg1930878
hg1830878
hg1730878
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5862
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)nssv3557
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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