A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6070



Internal ID15191108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:71367157..71617599hg38UCSC Ensembl
Outerchr6:72076860..72327302hg19UCSC Ensembl
Outerchr6:72133581..72384023hg18UCSC Ensembl
Outerchr6:72133581..72384023hg17UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38250443
hg19250443
hg18250443
hg17250443
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7382
Supporting Variants
SamplesNA12156
Known GenesLINC00472, MIR30A, MIR30C2
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)nssv6070
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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