A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5702



Internal ID15203852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:36941568..36972804hg38UCSC Ensembl
Outerchr7:36981173..37012409hg19UCSC Ensembl
Outerchr7:36947698..36978934hg18UCSC Ensembl
Outerchr7:36754413..36785649hg17UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg388043
hg198043
hg188043
hg178043
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4975
SamplesNA19129
Known GenesELMO1
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)nsv5702
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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