A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5574



Internal ID15203711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:161175785..161209095hg38UCSC Ensembl
Outerchr6:161596817..161630127hg19UCSC Ensembl
Outerchr6:161516807..161550117hg18UCSC Ensembl
Outerchr6:161567228..161600538hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg385968
hg195968
hg185968
hg175968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4952
SamplesNA19129
Known GenesAGPAT4
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)nsv5574
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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