A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv436



Internal ID15544937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:186410886..186439157hg38UCSC Ensembl
Outerchr4:187332040..187360311hg19UCSC Ensembl
Outerchr4:187569034..187597305hg18UCSC Ensembl
Outerchr4:187707189..187735460hg17UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg387991
hg197991
hg187991
hg177991
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4645
Supporting Variants
SamplesNA19240
Known GenesF11-AS1
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)nssv436
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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