A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6774



Internal ID15205031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:137786306..137830601hg38UCSC Ensembl
Outerchr9:140680758..140725053hg19UCSC Ensembl
Outerchr9:139800579..139844874hg18UCSC Ensembl
Outerchr9:137956595..138000890hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3844296
hg1944296
hg1844296
hg1744296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1817
SamplesNA18555
Known GenesEHMT1
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)nsv6774
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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