A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv61



Internal ID15037143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1878156..1919990hg38UCSC Ensembl
Outerchr11:1899386..1941220hg19UCSC Ensembl
Outerchr11:1855962..1897796hg18UCSC Ensembl
Outerchr11:1855962..1897796hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3841835
hg1941835
hg1841835
hg1741835
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv61
SamplesNA15510
Known GenesLSP1, TNNT3
MethodSequencing
AnalysisFosmids were categorized as discordant if the in silico size was in excess of three standard deviations from the mean (<32 or 48> kb) and/or showed incorrect orientation of ends
PlatformCapillary
Comments
ReferenceTuzun_et_al_2005
Pubmed ID15895083
Accession Number(s)nsv61
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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