A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9187



Internal ID15187991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:59561445..59606320hg38UCSC Ensembl
Outerchr1:60027117..60071992hg19UCSC Ensembl
Outerchr1:59799705..59844580hg18UCSC Ensembl
Outerchr1:59739138..59784013hg17UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg3844876
hg1944876
hg1844876
hg1744876
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1043
Supporting Variants
SamplesNA12156
Known GenesFGGY
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)nssv9187
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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