A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7611



Internal ID15552638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:128686316..128730976hg38UCSC Ensembl
Outerchr10:130484580..130529240hg19UCSC Ensembl
Outerchr10:130374570..130419230hg18UCSC Ensembl
Outerchr10:130374570..130419230hg17UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3844661
hg1944661
hg1844661
hg1744661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8865
SamplesNA12156
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)nsv7611
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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