A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv16



Internal ID15036955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:143593922..143909128hg38UCSC Ensembl
Outerchr7:143291015..143606221hg19UCSC Ensembl
Outerchr7:143001137..143237154hg18UCSC Ensembl
Outerchr7:142807852..143043869hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38315207
hg19315207
hg18236018
hg17236018
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16
SamplesNA15510
Known GenesCTAGE6, FAM115A, FAM115C, LOC154761
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)nsv16
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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