A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9697



Internal ID15540106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:106683130..106722671hg38UCSC Ensembl
Outerchr6:107131005..107170546hg19UCSC Ensembl
Outerchr6:107237698..107277239hg18UCSC Ensembl
Outerchr6:107237698..107277239hg17UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3839542
hg1939542
hg1839542
hg1739542
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7383
Supporting Variants
SamplesNA18507
Known GenesLOC100422737
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)nssv9697
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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