A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3918



Internal ID15201889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:99857024..99873236hg38UCSC Ensembl
Outerchr3:99575868..99592080hg19UCSC Ensembl
Outerchr3:101058558..101074770hg18UCSC Ensembl
Outerchr3:101058558..101074770hg17UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg387678
hg197678
hg187678
hg177678
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10354
SamplesNA18956
Known GenesCMSS1, FILIP1L, MIR548G
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)nsv3918
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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