A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7599



Internal ID15552624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:125669065..125701886hg38UCSC Ensembl
Outerchr10:127357634..127390455hg19UCSC Ensembl
Outerchr10:127347624..127380445hg18UCSC Ensembl
Outerchr10:127347624..127380445hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3832822
hg1932822
hg1832822
hg1732822
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8861
SamplesNA12156
Known GenesLOC283038, TEX36
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)nsv7599
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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