A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576



Internal ID15551499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:48267463..48296212hg38UCSC Ensembl
Outerchr10:49475506..49504255hg19UCSC Ensembl
Outerchr10:49145512..49174261hg18UCSC Ensembl
Outerchr10:49145512..49174261hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3810753
hg1910753
hg1810753
hg1710753
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10758
SamplesNA18956
Known GenesFRMPD2
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)nsv6576
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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