A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8592



Internal ID15535272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:35755370..35800190hg38UCSC Ensembl
Outerchr10:36044298..36089118hg19UCSC Ensembl
Outerchr10:36084304..36129124hg18UCSC Ensembl
Outerchr10:36084304..36129124hg17UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3844821
hg1944821
hg1844821
hg1744821
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6354
Supporting Variants
SamplesNA12156
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)nssv8592
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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