A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8847



Internal ID15188331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:113585355..113630190hg38UCSC Ensembl
Outerchr10:115345114..115389949hg19UCSC Ensembl
Outerchr10:115335104..115379939hg18UCSC Ensembl
Outerchr10:115335104..115379939hg17UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3844836
hg1944836
hg1844836
hg1744836
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7555
Supporting Variants
SamplesNA12156
Known GenesHABP2, NRAP
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)nssv8847
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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