A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6742



Internal ID15204996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:23927423..23960891hg38UCSC Ensembl
Outerchr1:24253913..24287381hg19UCSC Ensembl
Outerchr1:24126500..24159968hg18UCSC Ensembl
Outerchr1:23999219..24032687hg17UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg386557
hg196557
hg186557
hg176557
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2882
SamplesNA18555
Known GenesMIR378F, PNRC2
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)nsv6742
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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