A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10588



Internal ID15542210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:155475174..155506986hg38UCSC Ensembl
Outerchr7:155267869..155299681hg19UCSC Ensembl
Outerchr7:154960630..154992442hg18UCSC Ensembl
Outerchr7:154767345..154799157hg17UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg387674
hg197674
hg187674
hg177674
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6017
Supporting Variants
SamplesNA18956
Known GenesCNPY1
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)nssv10588
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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