A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17572347



Internal ID21764390
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 StatusS
Merged Variantsnsv6101679
Supporting Variants
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)nssv17572347
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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