A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5355



Internal ID15550156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:75957028..75988567hg38UCSC Ensembl
Outerchr6:76666745..76698284hg19UCSC Ensembl
Outerchr6:76723465..76755004hg18UCSC Ensembl
Outerchr6:76723465..76755004hg17UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg388207
hg198207
hg188207
hg178207
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3449
SamplesNA12878
Known GenesIMPG1
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)nsv5355
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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