A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5754



Internal ID8517577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:8037078..8070202hg38UCSC Ensembl
Outerchr10:8079041..8112165hg19UCSC Ensembl
Outerchr10:8119047..8152171hg18UCSC Ensembl
Outerchr10:8119047..8152171hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg386618
hg196618
hg186618
hg176618
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3864
SamplesNA12878
Known GenesGATA3, GATA3-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)nsv5754
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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