A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5277



Internal ID15203384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:41112016..41146182hg38UCSC Ensembl
Outerchr6:41079755..41113920hg19UCSC Ensembl
Outerchr6:41187733..41221898hg18UCSC Ensembl
Outerchr6:41187733..41221898hg17UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg385262
hg195262
hg185262
hg175262
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8242
SamplesNA12156
Known GenesADCY10P1
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)nsv5277
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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