A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3582



Internal ID15538310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:137115328..137140801hg38UCSC Ensembl
Outerchr7:136800075..136825548hg19UCSC Ensembl
Outerchr7:136450615..136476088hg18UCSC Ensembl
Outerchr7:136257330..136282803hg17UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg386346
hg196346
hg186346
hg176346
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5962
Supporting Variants
SamplesNA12878
Known GenesLOC349160
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)nssv3582
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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