A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6176



Internal ID15551059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:27553250..27585872hg38UCSC Ensembl
Outerchr10:27842179..27874801hg19UCSC Ensembl
Outerchr10:27882185..27914807hg18UCSC Ensembl
Outerchr10:27882185..27914807hg17UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg386872
hg196872
hg186872
hg176872
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10720
SamplesNA18956
Known Genes
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)nsv6176
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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