A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv855



Internal ID15552876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:52155519..52187874hg38UCSC Ensembl
Outerchr1:52621191..52653546hg19UCSC Ensembl
Outerchr1:52393779..52426134hg18UCSC Ensembl
Outerchr1:52333212..52365567hg17UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg386912
hg196912
hg186912
hg176912
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5571
SamplesNA19129
Known GenesZFYVE9
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)nsv855
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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