A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3



Internal ID15383497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:91388391..91416419hg38UCSC Ensembl
Outerchr7:91017706..91045734hg19UCSC Ensembl
Outerchr7:90855642..90883670hg18UCSC Ensembl
Outerchr7:90662357..90690385hg17UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3828029
hg1928029
hg1828029
hg1728029
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3
Supporting Variants
SamplesNA15510
Known Genes
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)nssv3
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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