A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101679



Internal ID22010913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155644040..159098501hg38UCSC Ensembl
chr7:155436734..158891192hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg383454462
hg193454459
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17572347
Samples
Known GenesC7orf13, DNAJB6, ESYT2, LINC00244, LINC00689, LINC01006, LMBR1, LOC100506585, LOC285889, MIR153-2, MIR5707, MIR595, MNX1, MNX1-AS1, NCAPG2, NOM1, PTPRN2, RBM33, RNF32, SHH, UBE3C, VIPR2, WDR60
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101679
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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