A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584



Internal ID15551508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:81932956..81991537hg38UCSC Ensembl
Outerchr9:84547871..84606452hg19UCSC Ensembl
Outerchr9:83737691..83796272hg18UCSC Ensembl
Outerchr9:81777425..81836006hg17UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3858582
hg1958582
hg1858582
hg1758582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv812
SamplesNA19240
Known GenesSPATA31D1, SPATA31D3, SPATA31D4
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)nsv6584
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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