A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7109



Internal ID15536755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:97151806..97184806hg38UCSC Ensembl
Outerchr4:98072957..98105957hg19UCSC Ensembl
Outerchr4:98291980..98324980hg18UCSC Ensembl
Outerchr4:98430135..98463135hg17UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg386429
hg196429
hg186429
hg176429
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4435
Supporting Variants
SamplesNA12156
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)nssv7109
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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