A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6764



Internal ID15205020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:136342675..136387661hg38UCSC Ensembl
Outerchr9:139237127..139282113hg19UCSC Ensembl
Outerchr9:138356948..138401934hg18UCSC Ensembl
Outerchr9:136512964..136557950hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3844987
hg1944987
hg1844987
hg1744987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8675
SamplesNA12156
Known GenesCARD9, DNLZ, GPSM1, SNAPC4
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)nsv6764
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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