A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6751



Internal ID15205006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:134102353..134142009hg38UCSC Ensembl
Outerchr9:136967475..137007131hg19UCSC Ensembl
Outerchr9:135957296..135996952hg18UCSC Ensembl
Outerchr9:133997029..134036685hg17UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3839657
hg1939657
hg1839657
hg1739657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6300, nssv1809
SamplesNA12156, NA18555
Known GenesWDR5
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)nsv6751
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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