A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604



Internal ID15551530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:88242106..88288212hg38UCSC Ensembl
Outerchr9:90857021..90903127hg19UCSC Ensembl
Outerchr9:90046841..90092947hg18UCSC Ensembl
Outerchr9:88086575..88132681hg17UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg3846107
hg1946107
hg1846107
hg1746107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6287, nssv5168
SamplesNA12156, NA19129
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)nsv6604
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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