A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9727



Internal ID15193270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:112720560..121600635hg38UCSC Ensembl
Outerchr7:112360615..121240689hg19UCSC Ensembl
Outerchr7:112147851..121027925hg18UCSC Ensembl
Outerchr7:111954566..120834640hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg388880076
hg198880075
hg188880075
hg178880075
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7405
Supporting Variants
SamplesNA18507
Known GenesANKRD7, ASZ1, C7orf60, CAPZA2, CAV1, CAV2, CFTR, CPED1, CTTNBP2, FAM3C, FOXP2, GPR85, ING3, KCND2, LINC00998, MDFIC, MET, MIR3666, MIR6132, NAA38, PPP1R3A, ST7, ST7-AS1, ST7-AS2, ST7-OT3, ST7-OT4, TES, TFEC, TMEM168, TSPAN12, WNT16, WNT2
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)nssv9727
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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